Looking forward to Treakisym Phase III data

SymBio Pharmaceuticals 18 April 2019 ADR Outlook
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SymBio Pharmaceuticals

Looking forward to Treakisym Phase III data

Corporate outlook

Pharma & biotech

18 April 2019

ADR research

Price

US$1.98*

Market cap

US$173m

*Underlying ¥ price converted at ¥113/US$

ADR/Ord conversion ratio 1:1

Net cash (US$m) at end December 2018

43

ADRs in issue

87.3m

ADR code

SYMQY

ADR exchange

OTC

Underlying exchange

Tokyo

Depository

BNY

Business description

SymBio Pharmaceuticals is a Japanese specialty pharma company with a focus on oncology and hematology. The Treakisym powder formulation was in-licensed from Astellas in 2005; liquid Treakisym was in-licensed from Eagle Pharmaceuticals in 2017. Rigosertib was in-licensed from Onconova.

Next events

Treakisym sales update

Q219

DLBCL top-line data

H219

RTD liquid formulation filing

2019

Analysts

Dr Dennis Hulme

+61 (0)2 9258 1161

Maxim Jacobs

+1 646 653 7027

SymBio Pharmaceuticals is a research client of Edison Investment Research Limited

Treakisym continues to generate double-digit sales growth, although 2018 sales were below our expectations. A temporary dip in revenue is expected in 2020 as inventory held by Eisai is wound down, ahead of SymBio establishing its own sales organization in Japan at the end of that year. The ongoing Phase III study of Treakisym in diffuse large B-cell lymphoma (DLBCL) is on track to allow a potential filing in Q220; we estimate that the DLBCL indication could double peak sales, if approved. SymBio reaffirmed its key goal to become profitable in 2021, the first full year of Treakisym self-commercialization. Our valuation is $237m or $2.7/ADR.

Year end

Revenue (US$m)

PTP
(US$m)

EPADR
($)

DPADR
($)

P/E
(x)

Gross yield
(%)

12/17

30.5

(35.2)

(0.71)

0.0

N/A

N/A

12/18

33.9

(24.3)

(0.37)

0.0

N/A

N/A

12/19e

36.4

(32.6)

(0.36)

0.0

N/A

N/A

12/20e

29.1

(46.9)

(0.48)

0.0

N/A

N/A

Note: Converted at ¥113 to US$1.

Guidance adjusted for lower sales, lower costs

Treakisym sales reported by partner Eisai rose by ~12% to ~$67m in 2018. SymBio’s revenue from Eisai and other partners rose by 11.4% to $34m, but was 9% below guidance and our forecasts. Net loss declined by 31% to $25m. The company’s updated mid-range plan forecasts sales to decline by 26% in 2020 to ~$29m, as it transitions the product shipment destination from Eisai to wholesalers, ahead of the switch to the company’s own salesforce in 2021. Its 2021 sales target is lowered by about 17% to $81m. However, lower anticipated costs mean that targeted net profit in 2021, the first full year of self-commercialization, is virtually unchanged at $9m.

First Treakisym liquid formulation to file Q121

SymBio is on track to launch its ready-to-dilute (RTD) liquid Treakisym formulation in Q121 and is preparing a marketing application for filing. A trial to confirm the safety of the rapid-infusion (RI) product enrolled the first subject in April 2019, with a market launch targeted in H122. SymBio aims to transition at least 90% of patients from currently marketed freeze dried (FD) powder to liquid formulations by the end of 2021, and 100% by end 2022. This strategy could prevent FD generics from gaining significant market share (generics not expected before June 2022).

Treakisym on track for DLBCL filing in Q220

The Phase III study of Treakisym in DLBCL recently completed recruitment; if the trial is successful, filing is planned for Q220, allowing a potential launch in Q321.

Valuation: rNPV of $237m (¥26.8bn) or $2.7/ADR

Our updated SymBio risk-adjusted valuation is $237m or $2.7/ADR (vs $225m). The increase results from the $38m net capital raised in 2018 and rolling forward the model, partly offset by lower peak sales in currently approved Treakisym indications and the sales dip in 2020 due to inventory run-off.

Investment summary

Company description: Japanese specialty pharma company

SymBio is a Japanese specialty pharma company that was established in 2005 and is based in Tokyo. It in-licenses assets with proof-of-concept data for development and commercialization in Asia-Pacific, removing the need for investment in early-stage R&D. SymBio has two main assets: Treakisym (bendamustine) for blood cancers, with Asia-Pacific marketing rights out-licensed to various commercial partners; and rigosertib for a rare blood cancer, which is being investigated in a global Phase III trial in which SymBio is participating. SymBio plans to commercialize Treakisym and rigosertib via its own salesforce after 2020 in Japan. SymBio is exploring opportunities to in-license further assets during 2019. It is also looking to expand globally and it established a US-based subsidiary in 2016.

Exhibit 1: SymBio main product pipeline

Product

Indication(s)

Stage

Comments

Treakisym (SyB L-0501)

r/r lg NHL/MCL

Marketed

First approved indication in Japan. Partner Eisai reported 2018 sales of $67m.

CLL; first-line lg NHL/MCL

Marketed

Both indications were approved in Japan during 2016 launched by partner Eisai in 2017.

r/r DLBCL

Phase III

Phase III initiated Q317, fully recruited Q219; targeting filing Q220, launch Q321.

Rigosertib iv (SyB L-1101)

r/r HR-MDS

Phase III

Global Phase III ongoing with SymBio participating; trial expanded after cleared interim analysis in Q118; full recruitment expected H219; SymBio targeting filing in 2021.

Rigosertib oral (SyB C-1101)

First-line HR-MDS (combo) and LR-MDS

Phase I

New Phase I single agent study of oral high-dose rigosertib initiated Q217, to be followed by Phase I in combination with Vidaza; SymBio intends to participate in partner Onconova’s planned Phase III combo trial in first-line HR-MDS.

Source: Edison Investment Research. Note: NHL: non-Hodgkin’s lymphoma; MCL: mantle cell lymphoma; CLL: chronic lymphocytic leukemia; lg: low grade; r/r: relapsed/refractory; DLBCL: diffuse large B-cell lymphoma; HR-MDS: higher-risk myelodysplastic syndromes; LR-MDS: lower-risk myelodysplastic syndromes.

Valuation: Risk-adjusted NPV of $237m (¥26.8bn) or $2.7/ADR

We value SymBio at $237m (¥26,828m) or $2.7/ADR, which is based on a risk-adjusted NPV analysis and includes $43m net cash at end December 2018. Our valuation includes Treakisym, where we assume sales can continue to grow for the next two years supported by additional indications that were approved in 2016, as well as risk-adjusted contributions for the relapsed/refractory (r/r) DLBCL indication for Treakisym (Phase III ongoing) and for rigosertib. Our valuation assumes that liquid Treakisym formulations will allow SymBio to maintain a greater than 75% share of the market until at least 2031 in the face of competition from powder generics from 2022 onwards.

Financials: Cash runway to H120

We estimate that end December 2018 net cash of $43m should be sufficient to fund operations into H120. We model $37m of indicative debt in FY20, and note that the company may require additional funding over and above these amounts for investment in new in-licensing or M&A opportunities.

Sensitivities: Treakisym sales growth and pipeline progress

The main sensitivities for SymBio relate to the main assets and SymBio’s ability to in-license additional products in the future. For Treakisym, our estimates assume that partner Eisai can continue to grow sales over the next two years in the indications that were approved in 2016. We also expect top-line data from Treakisym in r/r DLBCL during 2019, which will be critical in shaping the future development pathway. SymBio plans to establish its own salesforce to market Treakisym and rigosertib (if approved), which will require investment into a commercial infrastructure from 2019 onwards. We estimate sales organization costs to be $15m per year.

Maximizing Treakisym’s potential

SymBio acquired the rights to develop and commercialize Treakisym from Astellas in Japan (2005) and subsequently in China/Hong Kong, Korea, Taiwan and Singapore (April 2007). In 2008, SymBio out-licensed the marketing of Treakisym to various commercial partners (an overview of the main agreements is shown in Exhibit 2). Although precise deal terms have not been disclosed, we estimate that SymBio earns an average net margin of around 10–12% on top-line reported Treakisym sales in Asia-Pacific. SymBio intends to establish its own sales organization to market Treakisym in Japan after the current marketing arrangement with Eisai expires in December 2020.

Exhibit 2: Summary of SymBio’s Treakisym commercial out-licensing deals

Region

Partner

Date

Terms

Taiwan

InnoPharmax

March 2008

Development and launch; SymBio receives upfront, milestones and double-digit royalty.

Japan

Eisai

August 2008

Co-development and commercialization rights; Eisai and SymBio share development costs equally, with Eisai funding 100% of sales and marketing.

South Korea, Singapore

Eisai

May 2009

Development and marketing rights (financials not disclosed).

China (including Hong Kong)

Cephalon (Teva)

April 2009

Development and commercialization rights (financials not disclosed).

Source: Edison Investment Research, SymBio

SymBio moved to extend the lifecycle of Treakisym when it in-licensed rights to patent-protected liquid formulations of Treakisym from Eagle in September 2017. The liquid formulations are protected by patents that extend to 2031. Treakisym is likely to face competition from generic versions of the marketed FD powder formulation from June 2022, but the company expects to switch the majority of patients to the more convenient liquid formulations following the intended launch of the RTD formulation in Q121.

Encouraged by the longer Treakisym lifecycle, SymBio is investing in a Phase III study of Treakisym in r/r DLBCL patients, an indication where it reported promising results from a Phase II study in 2012. DLBCL comprises around 45% of non-Hodgkin’s lymphoma (NHL) cases in Japan, and we estimate that approval in this indication could double the sales potential of Treakisym.

Taken together, the patented liquid formulations and the DLCBL Phase III justify SymBio investing in establishing its own sales organization to market Treakisym and other drugs such as rigosertib (if approved), in our view. We estimate that SymBio could earn an operating profit margin of 50% of net sales of Treakisym under a self-commercialization model, compared to an estimated margin of 10–12% of in-market top-line sales under the arrangement with Eisai. We expect the higher margin from self-commercialization of Treakisym to make SymBio profitable in 2021.

New products could leverage own sales organization

Having its own sales organization should enable SymBio to better understand and respond to market needs, positioning it to deliver the benefits of Treakisym to healthcare providers and patients. Treakisym is used in the hematology departments of approximately 900 institutions across Japan, with the top 400 institutions accounting for ~90% of sales. If rigosertib is approved for treating myelodysplastic syndromes (MDS), the top 400 institutions would similarly be expected to account for the majority of use. Therefore, SymBio would be in a position to market rigosertib (if approved) through its own sales organization for minimal additional cost. The same operation leverage would apply were SymBio to in-license or develop other hematological drugs. Establishing its own sales organization will be an important step towards achieving SymBio’s vision of establishing itself as a leading specialty pharma company.

Pipeline progress

Exhibit 3 summarizes the status of SymBio’s product pipeline. The main areas of focus are:

Obtaining approval for the two liquid formulations of Treakisym to extend the product lifecycle out to 2031.

Completion of the Phase III study of Treakisym in DLBCL, which could potentially double the sales potential of Treakisym.

Participating in the global Phase III study of intravenous (iv) rigosertib in MDS, which could become SymBio’s second product for hematological cancers.

Completion of ongoing Phase I studies of oral formulations of Treakisym and rigosertib, which could lead to development of additional indications for both drugs.

Exhibit 3: Status of Treakisym development program

Source: SymBio

Exhibit 4: Rigosertib development program

Source: SymBio

Key news anticipated for SymBio in 2019 includes:

Top-line data from the DLBCL Phase III study.

Filing for approval of the RTD liquid Treakisym formulation.

Update on the clinical study of the rapid infusion Treakisym formulation.

Reaching full recruitment in the rigosertib Phase III study.

Liquid formulations extend Treakisym lifecycle

The new liquid formulations of Treakisym that SymBio in-licensed from Eagle are more convenient for healthcare workers and for patients.

The first in-licensed product is an RTD liquid formulation that will significantly reduce dose preparation time, making it easier and safer for health professionals. This compares to the FD Treakisym, which has to be reconstituted before administration, a time-consuming process that carries the risk of exposing healthcare workers to cytotoxic powders and vapors.

The second in-licensed product is an RI formulation that will cut drug infusion time to 10 minutes from 60 for the current Treakisym product (and the RTD formulation).

Liquid formulations aim to maintain SymBio’s market share

We expect the approval pathway for the RTD Treakisym formulation to be relatively straightforward, as the same dose of drug is administered to patients in the same way, with the only difference being the way the dose is prepared. SymBio has consulted with regulators the approval pathway for the RTD formulation and is preparing a filing application. It has narrowed down the timing of the anticipated launch of the RTD product to Q121, which is towards the earlier end of its previous target of H121. A launch at this time would allow it the RTD formulation to be well established in the marketplace before the potential entry of the first FD generics in June 2022.

The RI product represents a greater change to the current treatment protocols, so approval of this product is expected to take longer. SymBio announced on 4 April 2019 that it had enrolled the first of the planned 32 patients in a clinical trial primarily aimed at confirming the safety of the RI formulation; market launch targeted in H122. We conservatively model a 95% chance of a launch of the RI product by the start of 2023.

SymBio aims to transition at least 90% of patients from currently marketed FD powder to liquid formulations by the end of 2021, and 100% by the end of 2022. We take a slightly more conservative view and model 95% of patients being switched to these products.

DLBCL indication could double Treakisym sales

SymBio is seeking to add another indication for Treakisym, in the treatment of r/r DLBCL, an intermediate or high-risk form of NHL. It commenced a Phase III trial to confirm the safety and efficacy of Treakisym plus rituximab in r/r DLBCL in August 2017 and announced on 8 April 2019 that it had completed enrolment. SymBio’s mid-range plan aims to file an NDA in Q220 and is targeting a market launch in Q321, if approved, so we expect top-line data to be reported in H219. We model Phase III costs of $18m and a potential launch in H221.

DLBCL is a rapidly growing, intermediate or high-risk form of NHL, in contrast to the slower-growing indolent or low-risk lymphomas that are included in the current approvals for Treakisym.

DLBCL is the most common form of NHL and is estimated to represent 45% of NHL cases in Japan.1 Based on epidemiology studies1 and Globocan data, we estimate there will be 35,500 new cases of NHL and 16,000 new cases of DLBCL in Japan in 2020. Assuming that 70% of DLBCL patients progress to receive second-line therapy, we forecast a target market of 11,200 second-line (r/r) DLBCL patients per year in Japan by 2020.

  Chihara et al; British Journal of Haematology, 2014, 164, 536–545.

The market of 11,200 r/r DLBCL patients in Japan is almost as large as the combined market of ~12,500 patients for the currently approved indications for Treakisym in chronic lymphocytic leukemia (CLL) and first-line and r/r low-grade NHL and mantle cell lymphoma (MCL). Given the high unmet need for this patient group, we model a 50% market penetration and peak sales (net sales after discounts) of $85m for DLBCL vs $82m for the currently approved indications.

Treakisym sales forecasts trimmed after slower 2018

Japan accounts for about 95% of Treakisym sales. Japanese in-market sales of Treakisym estimated from prescription numbers and expressed on a National Health Insurance price basis grew by 11.6% to ~$75m in 2018, from $67m in the previous year. Partner Eisai reports sales on a net sales after discounts basis; on this basis Eisai reported Treakisym sales revenue of $65m in Japan itself for the 2018 calendar year (up ~12%) and total net Treakisym revenue of $67m when sales in other territories (South Korea and Singapore) were included.

SymBio books revenue equal to about 50% of net in-market Treakisym sales under the marketing agreement with Eisai. While total sales reported by SymBio in 2018 increased by 11.4% to $34m, these sales were 9% below guidance and our forecasts.

Treakisym sales have grown by ~80% over the period from 2016 to 2018, supported by approvals for two new indications for Treakisym in Japan that were received in 2016:

CLL, approved in August 2016; and

first-line low-grade NHL and MCL (first-line lg NHL/MCL), approved in December 2016.

SymBio attributed the shortfall in 2018 sales to slower than expected market penetration in first-line treatment of low-grade NHL. As a result, it has reduced its targeted market penetration in first-line lg NHL to 70% by 2020, from its previous target of 75%.

We have adjusted our forecasts of net in-market sales of Treakisym in currently approved indications, adjusted for discounts (the form reported by Eisai), to grow by $5m in 2019 (75% of the Treakisym sales growth reported by Eisai for the 2018 calendar year) and by $5m in 2020. We forecast Treakisym sales in existing indications to peak at $76m (previously $84m) in 2021, as shown in Exhibit 5.

We model in-market Treakisym sales (net sales after discounts) in DLBCL in 2021 to be $4m, if launched in Q321 in line with the company’s targets. We estimate that sales in DLBCL could exceed the currently marketed indications by 2025, and peak at $85m in 2026, if approved (Exhibit 5).

Exhibit 5: Treakisym in-market net sales forecasts

Source: Eisai, SymBio, Edison Investment Research. Note: SymBio records royalties on in-market Treakisym sales; sales estimates are net in-market sales, after discounts.

Plans for self-commercialization starting to take shape

In February, SymBio released an updated four-year plan along with its results for the 2018 financial year. The plan provides a clearer outline of the pathway to self-commercialization in 2021. Previously, in February 2018 the company foreshadowed that it was giving serious consideration to moving to self-commercialization of Treakisym, and at that time prepared its 2021 targets on the assumption that it would proceed with self-commercialization. On 16 October 2018 it announced that it had begun preparations to establish its own sales organization to sell Treakisym in Japan.

The rationale for self-commercialization is underpinned by the in-license of liquid formulations of Treakisym from Eagle Pharmaceuticals. We expect the launch of liquid formulations (if approved) to allow SymBio to maintain a dominant share of the bendamustine hydrochloride market in the face of FD powder generic which could be launched as early as June 2022.

Exhibit 6 compares the targets in the most recent four-year plan announced in February 2019 to the targets announced 12 months earlier. For 2021, we compare the new targets to the median of the old high and low targets.

The most notable revision is that the sales target for 2020 has been reduced by 23% to $29m, due to its expectation that it will discontinue shipments to Eisai around the end of H120 as it transitions the product shipment destination from Eisai to wholesalers.

Furthermore, targeted sales for 2021 are 17% below the median point of the old sales target range. The twin contributors for this are, firstly, an anticipated launch date of the DLBCL indication now three months later (Q321) and, secondly, a 5% reduction in the peak uptake of Treakisym in the first-line l/g NHL indications approved in 2016.

For the first time the company has provided performance targets for 2022. These provide the first insights as to the company’s expectations of the full-year sales potential and the costs of promoting the DLBCL indication and liquid formulations for Treakisym. We calculate targeted operating expenses to be $82m in 2022 vs $70m in 2021, with lower R&D costs due to the completion of the DLBCL Phase III trial likely partly offsetting the cost of supporting its own sales force.

Exhibit 6: Old and new forecasts and performance targets

2019

2019

 

2020

2020

 

2021*

2021

 

2022**

2022

2022*

Old
($m)

New
($m)

% Change

Old
($m)

New
($m)

% Change

Old
(median, $m)

New
($m)

% Change

Low
($m)

High
($m)

Median
($m)

Revenue

37.5

39.5

+5%

37.5

29.0

-23%

97.1

80.8

-17%

99.8

104.5

102.2

Operating income

(33.5)

31.7

-195%

(33.5)

45.8

-237%

11.7

10.8

-8%

18.4

21.8

20.1

Ordinary income

(34.1)

32.0

-194%

(34.1)

46.2

-236%

11.3

10.5

-7%

18.1

21.4

19.7

Net income

(34.1)

32.0

-194%

(34.1)

46.3

-236%

9.6

8.9

-7%

15.4

18.2

16.8

Implied OpEx

(71.0)

(7.8)

-89%

(71.0)

16.8

-124%

(85.4)

(70.0)

-18%

(82.0)

Source: SymBio, Edison Investment Research. Note: *Median values calculated by Edison from high and low range data; ** 2022 performance targets have been provided or the first time in the current four-year mid-range plan; OpEx= operating expenses – calculated by Edison as revenue minus operating profit.

IV rigosertib: A potential second product for SymBio

SymBio in-licensed rigosertib (iv and oral formulations, Japan and Korean rights) from Onconova in 2011 for MDS, a rare blood cancer. SymBio is contributing patients from Japan to the global Phase III INSPIRE trial of iv rigosertib for the treatment of second-line higher-risk MDS (HR-MDS).

Onconova announced on 25 March 2019 that enrolment in the Phase III study has passed 75% (ie 270 patients), and that it is on track to fully enroll the target of 360 patients in H219. Onconova also expect to report top-line results of the overall survival analysis after 288 events will be available in H219. SymBio has previously said it aims to file for approval in Japan in 2021.

As of December 2018 SymBio had already reached its target of enrolling 40 patients in Japan, but it has stated that enrolment is proceeding.

Onconova said that the Independent Data Monitoring Committee had observed a promising survival signal at the interim analysis conducted in early 2018. The committee recommended that the trial continue with an expansion in enrolment to 360 patients (from 225 patients) based on a pre-planned sample size re-estimation.

Development of IONSYS pain patch terminated

SymBio in-licensed the exclusive rights to develop the IONSYS (SyB P-1501) pain patch in Japan from The Medicines Company (MDCO) in October 2015 and initiated a Phase III trial in Japan in June 2016. SymBio suspended enrolment in the trial in April 2017 due to concerns over the continuity of MDCO’s business regarding the product. The license agreement between SymBio and MDCO was terminated effective 30 November 2017 and SymBio completed the process of terminating the development of SyB P-1501 in February 2018. SymBio is seeking damages of at least $82m arising from MDCO’s repudiation of the license agreement. We do not include any potential damages in our valuation or forecasts.

Continued focus on in-licensing new drugs

SymBio is actively seeking new drug candidates and in-licensing opportunities globally, targeting drug candidates with clinically confirmed efficacy and safety. Discussions with multiple potential licensors are ongoing. If the company proceeds with its plans to establish its own salesforce in Japan, then there will be increased incentive to in-license additional products that could be marketed by the salesforce.

The company has established a US-based subsidiary, SymBio Pharma USA, as a strategic base for overseas business development. It may look to in-license or develop drugs it can commercialize on a global basis as part of a continued transformation to a global specialty pharma company.

Reverse stock split to take effect on 1 July

On 28 March, shareholders voted to approve a one-for-four consolidation of the company’s common stock, which will take effect on 1 July 2019. We will not incorporate the reverse stock split into our forecasts until after it takes effect on 1 July.

Sensitivities

SymBio is subject to the usual drug development risks, including clinical development delays or failures, regulatory risks, competitor successes, partnering setbacks, financing and commercial risks. The main sensitivities include rigosertib and DLBCL clinical trial success or failure, the ability to execute future in-licensing deals and successfully establishing its own salesforce to self-commercialize Treakisym after 2020.

For Treakisym, key risks relate to the outcome of the DLBCL Phase III trial, obtaining regulatory approval for the liquid Treakisym formulations and success in migrating patients to the liquid formulation to stave off competition from generic copies of Treakisym powder after 2021. It will have to bear the cost of establishing a salesforce before the marketing arrangement with Eisai expires.

SymBio is seeking damages from The Medicines Company arising from its repudiation of the IONSYS license agreement. We do not model any compensation payments for IONSYS, so if SymBio was to receive any compensation, this would represent the potential to recover some of the value we have now written off.

The main sensitivity for rigosertib is the outcome of the Phase III INSPIRE trial of iv rigosertib in second-line HR-MDS. Onconova may need additional cash to complete the trial and report top-line data. If it is unable to secure any additional funds that may be required, this could delay trial completion and therefore timelines. If the outcome of the trial is negative, then not only would this impact the development of iv rigosertib, but there could also be read-across to oral rigosertib.

SymBio is reliant on in-licensing further assets to fill its pipeline. We believe the CEO’s network is crucial to securing future deals, although we have limited visibility on the potential terms and timing of any such agreements.

Valuation

Our valuation of SymBio is increased to $237m (¥26,828m), or $2.7/ADR, based on a risk-adjusted NPV analysis, which includes $43m net cash at end December 2018 vs $26m at the end of the previous year. We use a 10% discount rate for approved products and 12.5% elsewhere. Our valuation includes Treakisym approved indications and the new r/r DLBCL indication, plus rigosertib. We have rolled our valuation model forward to the new financial year and reduced forecast peak sales for approved Treakisym indications by 9% to $76m, following below-expectations growth in 2018.

The higher cash balance due to $38m (net) raised from the issue of shares and share acquisition rights in 2018, combined with rolling forward the model to the new financial year, has more than offset the negative impact of reduced peak sales forecast for the approved Treakisym indications.

Our main assumptions are summarized in Exhibit 7 below.

Exhibit 7: SymBio rNPV valuation

Product

Indication

Launch

Peak sales ($m)**

Value
($m)

Probability

rNPV
($m)

NPV/ADR ($/ADR)

Treakisym

LG NHL/MCL (r/r and 1st line); CLL

2010*

76

146.1

100-95%

140.0

1.6

Treakisym (DLBCL)

r/r DLBCL

2021

85

84.5

60%

44.7

0.5

Rigosertib (IV)

r/r HR-MDS

2023

34

19.6

50%

7.9

0.1

Rigosertib (oral)

First-line HR-MDS (combo)

2025

66

31.7

15%

2.2

0.0

Net cash at 31 December 2018

42.7

100%

42.7

0.5

Valuation

324.6

237.4

2.7

Source: Edison Investment Research. Note: *Treakisym was launched in 2010 in r/r low-grade NHL/MCL; it received approvals in Japan in CLL in August 2016 and in first-line, low-grade NHL/MCL in December 2016; **we present Treakisym peak sales estimates net of discounts, to align with sales reporting by Eisai.

We model a 95% likelihood that the RI Treakisym formulation will be launched before the end of 2022, thereby minimizing the penetration of generic copies of the FD Treakisym formulation. We model branded Treakisym market share gradually declining from 96% in 2022 to 75% in 2031, followed by a more rapid decline from 2032 after the liquid formulation patents expire.

Our Treakisym valuation assumes that SymBio earns an average net margin of 10–12% on top-line reported Treakisym sales until 2020. We assume that after 2020 the net operating margin gradually increases to reach 50% in 2024 and subsequent years as SymBio switches to self-commercialization of Treakisym via its own salesforce and the liquid formulations in-licensed from Eagle gain market share vs powder formulations.

We model $13m of development costs to achieve approval for the RTD and RI liquid formulations. We estimate that a salesforce of 60 would be needed to market Treakisym in Japan. At a fully-loaded cost of $250,000 per person, this would cost $15m.

Scenario analysis

In a scenario where the Treakisym market share declines to 50% by 2031 (vs 75% for the base case), our valuation would fall by around $18m ($0.2/ADR) to around $220m ($2.5/ADR). We currently assume stable Treakisym pricing apart from a 5% price cut in 2022 when FD powder generics are expected to enter the market. However, an additional price cut to Treakisym in the future could represent downside to our forecasts; a 10% price cut in 2020 would remove around $23m from our Treakisym rNPV, or $0.3/ADR.

Financials

Our financial forecasts have been updated to reflect FY18 reported financials and SymBio’s updated financial guidance for 2019 and targets for 2020–2022. The main changes to our forecasts are summarised in Exhibit 8.

We have reduced forecast revenue in 2019 because 2018 sales were 9% below our expectations, and our decision to reduce our peak sales forecast for Treakisym in the approved indications to $76m from $84m (expressed as net in-market sales after discounts). We have reduced forecast revenue in 2020 by 27%, reflecting the anticipated winding down of Eisai inventory in H220 in the lead up the end of the marketing arrangement in December 2020.

We have increased R&D expenditure and reduced SG&A forecasts in 2019, broadly in line with SymBio’s guidance (Exhibit 9). We have increased forecast R&D expenditure in 2020 in line with the three-month delay in anticipated completion of the DLBCL Phase III, and have further increased forecast SG&A spend as SymBio begins to build its own salesforce in Japan.

SymBio raised $38m (net) from the issue of shares and share acquisition rights in 2018, lifting net cash at 31 December 2018 to $43m vs $26m at the end of the previous year. We estimate that the cash of $43m should be sufficient to fund operations into H120. We model $37m of indicative debt in FY20. The company may require additional funding over and above these amounts for investment in new in-licensing or M&A opportunities.

Exhibit 8: Main changes to our financial forecasts; ¥-based future financial forecasts

¥m

2019

2019

 

2020

2020

 

 

Old

New

% change

Old*

New

% change

Revenue

4,325

4,109

-5

4,502

3,293

-27

Research and development

(2,200)

(2,500)

+14

(1,767)

(2,623)

+48

Selling, general and administration

(2,720)

(2,436)

-10

(3,180)

(3,680)

+16

Operating profit (reported)

(3,640)

(3,703)

+2

(3,614)

(5,315)

+47

Profit before tax (reported)

(3,617)

(3,679)

+2

(3,602)

(5,303)

+47

Profit after tax (reported)

(3,621)

(3,683)

+2

(3,606)

(5,307)

+47

Source: Edison Investment Research. Note: *We have not previously published our 2020 forecasts.

Exhibit 9: SymBio’s 2018 outlook and 2019 targets versus our estimates; ¥-based future financial forecasts

 

2019
guidance

2019
estimates

2020
targets

2020
estimates

Revenue

¥4,465m

¥4,109m

¥3,282m

¥3,293m

R&D

¥2,508m

¥2,500m

N/A

¥2,623m

SG&A (including R&D)

¥5,053m

¥4,936m

N/A

¥6,303m

Operating loss

¥3,587m

¥3,703m

¥5,180m

¥5,315m

Ordinary loss

¥3,612m

¥3,679m

¥5,224m

¥5,303m

Net loss

¥3,616m

¥3,683m

¥5,228m

¥5,307m

Source: Edison Investment Research.

Exhibit 10: Financial summary

Accounts: JPN GAAP, year end: 31 December, $000s

 

2016

2017

2018

2019e

2020e

2021e

Total revenues

 

 

20,957

30,480

33,943

36,362

29,145

81,056

Cost of sales

 

 

(12,955)

(21,353)

(23,563)

(25,453)

(20,402)

(15,839)

Gross profit

 

 

8,002

9,126

10,379

10,909

8,744

65,217

SG&A (expenses)

 

 

(12,072)

(17,350)

(17,665)

(21,558)

(32,565)

(48,997)

R&D costs

 

 

(14,753)

(26,706)

(16,219)

(22,124)

(23,212)

(6,637)

Other income/(expense) included in adjusted

 

 

0

0

0

0

0

0

Other income/(expense) excluded from adjusted

 

 

0

0

0

0

0

0

Reported EBIT

 

 

(18,823)

(34,930)

(23,505)

(32,773)

(47,034)

9,583

Finance income/ (expense)

 

 

48

27

6

214

104

67

Other income/(expense) included in adjusted

 

 

65

24

(0)

0

0

0

Other income/(expense) excluded from adjusted

 

 

(1,728)

(290)

(826)

0

0

0

Reported PBT

 

 

(20,437)

(35,169)

(24,325)

(32,559)

(46,930)

9,650

Income tax expense

 

 

(34)

(34)

(34)

(34)

(34)

(806)

Reported net income

 

 

(20,471)

(35,202)

(24,359)

(32,593)

(46,963)

8,844

Average number of ADRs - basic (m)

 

 

39.3

49.9

66.5

89.9

97.4

97.4

Basic Earnings per ADR (US$)

 

(0.52)

(0.71)

(0.37)

(0.36)

(0.48)

0.09

Adjusted EBITDA

 

 

(18,596)

(34,668)

(23,198)

(3,242)

(4,667)

1,000

Adjusted EBIT

 

 

(18,823)

(34,930)

(23,505)

(3,277)

(4,703)

958

Adjusted PBT

 

 

(20,503)

(35,193)

(24,325)

(3,256)

(4,693)

965

Adjusted Earnings per ADR (US$)

 

(0.52)

(0.71)

(0.37)

(0.36)

(0.48)

0.09

Adjusted diluted Earnings per ADR (US$)

 

(0.52)

(0.71)

(0.37)

(0.36)

(0.48)

0.08

BALANCE SHEET

 

 

 

 

 

 

 

 

Property, plant and equipment

 

 

660

414

504

631

654

1,035

Goodwill

 

 

0

0

0

0

0

0

Intangible assets

 

 

372

610

632

524

446

391

Other non-current assets

 

 

680

886

643

643

643

643

Total non-current assets

 

 

1,711

1,909

1,778

1,798

1,743

2,068

Cash and equivalents

 

 

50,613

26,080

42,667

10,370

4,425

8,702

Inventories

 

 

2,413

3,208

4,724

2,092

1,677

1,302

Trade and other receivables

 

 

4,314

4,335

3,644

4,184

3,194

8,883

Other current assets

 

 

1,818

2,098

2,403

2,403

2,403

2,403

Total current assets

 

 

59,159

35,721

53,438

19,049

11,699

21,290

Non-current loans and borrowings

 

 

3,982

0

0

0

37,478

37,478

Trade and other payables

 

 

0

0

0

0

0

0

Other non-current liabilities

 

 

12

12

11

11

11

11

Total non-current liabilities

 

 

3,995

12

11

11

37,489

37,489

Trade and other payables

 

 

2,848

5,349

6,426

3,561

4,554

4,538

Current loans and borrowings

 

 

0

0

0

0

0

0

Other current liabilities

 

 

5,489

3,603

5,400

5,400

5,400

5,400

Total current liabilities

 

 

8,337

8,951

11,826

8,962

9,955

9,939

Equity attributable to company

 

 

48,539

28,667

43,379

11,874

(34,001)

(24,069)

Non-controlling interest

 

 

0

0

0

0

0

0

CASH FLOW STATEMENT

 

 

 

 

 

 

 

 

Profit before tax

 

 

(20,437)

(35,169)

(24,325)

(32,559)

(46,930)

9,650

Depreciation and Amortization

 

 

227

262

307

353

366

419

Share based payments

 

 

1,212

1,073

1,088

1,088

1,088

1,088

Other adjustments

 

 

1,744

370

755

(214)

(104)

(67)

Movements in working capital

 

 

(111)

(307)

1,633

(773)

2,398

(5,330)

Net cash from operating activities (pre-tax)

 

 

(17,365)

(33,771)

(20,542)

(32,105)

(43,181)

5,760

Interest paid / received

 

 

53

28

5

214

104

67

Income taxes paid

 

 

(34)

(34)

(34)

(34)

(34)

(806)

Cash from operations (CFO)

 

 

(17,346)

(33,777)

(20,571)

(31,925)

(43,110)

5,021

Capex

 

 

(247)

(505)

(352)

(372)

(312)

(744)

Acquisitions & disposals net

 

 

0

0

0

0

0

0

Other investing activities

 

 

(141)

(181)

120

0

0

0

Cash used in investing activities (CFIA)

 

 

(388)

(686)

(232)

(372)

(312)

(744)

Net proceeds from issue of shares

 

 

28,550

10,303

37,806

0

0

0

Movements in debt

 

 

3,982

0

0

0

37,478

0

Other financing activities

 

 

(159)

0

0

0

0

0

Cash from financing activities (CFF)

 

 

32,373

10,303

37,806

0

37,478

0

Currency translation differences and other

 

 

(1,738)

(373)

(416)

0

0

0

Increase/(decrease) in cash and equivalents

 

 

12,902

(24,533)

16,587

(32,297)

(5,945)

4,277

Cash and equivalents at end of period

 

 

50,613

26,080

42,667

10,370

4,425

8,702

Net (debt) cash

 

 

46,631

26,080

42,667

10,370

(33,053)

(28,776)

Source: Edison Investment Research and SymBio accounts. Note: Solely for the convenience of the reader the financial summary table has been converted at a rate of ¥113 to $1. SymBio reports statutory accounts in Japanese yen. These translations should not be considered representations that any such amounts have been or could be converted into US dollars at the assumed conversion rate.

Contact details

Revenue by geography

Toranomon 30 Mori Bldg
3-2-2 Toranomon
Minato-ku
Tokyo 105-0001
Japan
+81 3 5472-1125
www.symbiopharma.com

N/A

Contact details

Toranomon 30 Mori Bldg
3-2-2 Toranomon
Minato-ku
Tokyo 105-0001
Japan
+81 3 5472-1125
www.symbiopharma.com

Revenue by geography

N/A

Management team

President and CEO: Fuminori Yoshida

Corporate Officer and CFO: Kenji Murata

Mr Yoshida founded SymBio in March 2005. He has held senior management positions in the healthcare industry in both the US and Japan, including founding director of both Nippon BioRad Laboratories (1980) and Amgen Japan (1993) in addition to Amgen Inc as corporate VP. Mr Yoshida has a BS in organic chemistry (Gakushin University), an MS in molecular biology (MIT) and an MS in health policy and management (Harvard Grad School).

Mr Murata was the CFO for Japan at Novartis Pharma and, most recently before joining SymBio, at Elanco Japan. He has also held managerial roles at Novartis Japan Sourcing and Sumitomo Life Insurance.

Corporate Officer, Executive VP and COO: Kazuo Asakawa

Corporate Officer and CDO: Nobuo Ishida

Mr Asakawa is a SymBio corporate officer, executive VP and COO, as well as GM of SymBio’s Japan business unit. He was formerly MD and head of the Oncology division at Novartis Pharma KK, as well as being the company’s corporate officer, head of the Transplantation & Immunology business division, and GM of the marketing department. He has also held managerial roles at Nippon Roche and Sandoz Japan.

Mr Ishida is a SymBio corporate officer and chief development officer, as well as being head of R&D and director of R&D Support and Data Science. He was formerly oncology project head, Japan development, at AbbVie GK; also formerly global project leader, Oncology, R&D, at Bayer Healthcare.

Management team

President and CEO: Fuminori Yoshida

Mr Yoshida founded SymBio in March 2005. He has held senior management positions in the healthcare industry in both the US and Japan, including founding director of both Nippon BioRad Laboratories (1980) and Amgen Japan (1993) in addition to Amgen Inc as corporate VP. Mr Yoshida has a BS in organic chemistry (Gakushin University), an MS in molecular biology (MIT) and an MS in health policy and management (Harvard Grad School).

Corporate Officer and CFO: Kenji Murata

Mr Murata was the CFO for Japan at Novartis Pharma and, most recently before joining SymBio, at Elanco Japan. He has also held managerial roles at Novartis Japan Sourcing and Sumitomo Life Insurance.

Corporate Officer, Executive VP and COO: Kazuo Asakawa

Mr Asakawa is a SymBio corporate officer, executive VP and COO, as well as GM of SymBio’s Japan business unit. He was formerly MD and head of the Oncology division at Novartis Pharma KK, as well as being the company’s corporate officer, head of the Transplantation & Immunology business division, and GM of the marketing department. He has also held managerial roles at Nippon Roche and Sandoz Japan.

Corporate Officer and CDO: Nobuo Ishida

Mr Ishida is a SymBio corporate officer and chief development officer, as well as being head of R&D and director of R&D Support and Data Science. He was formerly oncology project head, Japan development, at AbbVie GK; also formerly global project leader, Oncology, R&D, at Bayer Healthcare.

Principal shareholders

(%)

Yoshida Fuminori

4.2

Cephalon

3.1

Matsui Securities

1.5

Japan Securities Finance Co.

1.5

Eisai Co., Ltd.

1.0

Companies named in this report

Eisai (4523 JP), Onconova (ONTX US), The Medicines Company (MDCO US)


General disclaimer and copyright

This report has been commissioned by SymBio Pharmaceuticals and prepared and issued by Edison, in consideration of a fee payable by SymBio Pharmaceuticals. Edison Investment Research standard fees are £49,500 pa for the production and broad dissemination of a detailed note (Outlook) following by regular (typically quarterly) update notes. Fees are paid upfront in cash without recourse. Edison may seek additional fees for the provision of roadshows and related IR services for the client but does not get remunerated for any investment banking services. We never take payment in stock, options or warrants for any of our services.

Accuracy of content: All information used in the publication of this report has been compiled from publicly available sources that are believed to be reliable, however we do not guarantee the accuracy or completeness of this report and have not sought for this information to be independently verified. Opinions contained in this report represent those of the Edison analyst at the time of publication. Forward-looking information or statements in this report contain information that is based on assumptions, forecasts of future results, estimates of amounts not yet determinable, and therefore involve known and unknown risks, uncertainties and other factors which may cause the actual results, performance or achievements of their subject matter to be materially different from current expectations.

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This Communication is being distributed in the United Kingdom and is directed only at (i) persons having professional experience in matters relating to investments, i.e. investment professionals within the meaning of Article 19(5) of the Financial Services and Markets Act 2000 (Financial Promotion) Order 2005, as amended (the "FPO") (ii) high net-worth companies, unincorporated associations or other bodies within the meaning of Article 49 of the FPO and (iii) persons to whom it is otherwise lawful to distribute it. The investment or investment activity to which this document relates is available only to such persons. It is not intended that this document be distributed or passed on, directly or indirectly, to any other class of persons and in any event and under no circumstances should persons of any other description rely on or act upon the contents of this document (nor will such persons be able to purchase shares in the placing).

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Frankfurt +49 (0)69 78 8076 960

Schumannstrasse 34b

60325 Frankfurt

Germany

London +44 (0)20 3077 5700

280 High Holborn

London, WC1V 7EE

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New York +1 646 653 7026

1,185 Avenue of the Americas

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Level 4, Office 1205

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Frankfurt +49 (0)69 78 8076 960

Schumannstrasse 34b

60325 Frankfurt

Germany

London +44 (0)20 3077 5700

280 High Holborn

London, WC1V 7EE

United Kingdom

New York +1 646 653 7026

1,185 Avenue of the Americas

3rd Floor, New York, NY 10036

United States of America

Sydney +61 (0)2 8249 8342

Level 4, Office 1205

95 Pitt Street, Sydney

NSW 2000, Australia

General disclaimer and copyright

This report has been commissioned by SymBio Pharmaceuticals and prepared and issued by Edison, in consideration of a fee payable by SymBio Pharmaceuticals. Edison Investment Research standard fees are £49,500 pa for the production and broad dissemination of a detailed note (Outlook) following by regular (typically quarterly) update notes. Fees are paid upfront in cash without recourse. Edison may seek additional fees for the provision of roadshows and related IR services for the client but does not get remunerated for any investment banking services. We never take payment in stock, options or warrants for any of our services.

Accuracy of content: All information used in the publication of this report has been compiled from publicly available sources that are believed to be reliable, however we do not guarantee the accuracy or completeness of this report and have not sought for this information to be independently verified. Opinions contained in this report represent those of the Edison analyst at the time of publication. Forward-looking information or statements in this report contain information that is based on assumptions, forecasts of future results, estimates of amounts not yet determinable, and therefore involve known and unknown risks, uncertainties and other factors which may cause the actual results, performance or achievements of their subject matter to be materially different from current expectations.

Exclusion of Liability: To the fullest extent allowed by law, Edison shall not be liable for any direct, indirect or consequential losses, loss of profits, damages, costs or expenses incurred or suffered by you arising out or in connection with the access to, use of or reliance on any information contained on this note.

No personalised advice: The information that we provide should not be construed in any manner whatsoever as, personalised advice. Also, the information provided by us should not be construed by any subscriber or prospective subscriber as Edison’s solicitation to effect, or attempt to effect, any transaction in a security. The securities described in the report may not be eligible for sale in all jurisdictions or to certain categories of investors.

Investment in securities mentioned: Edison has a restrictive policy relating to personal dealing and conflicts of interest. Edison Group does not conduct any investment business and, accordingly, does not itself hold any positions in the securities mentioned in this report. However, the respective directors, officers, employees and contractors of Edison may have a position in any or related securities mentioned in this report, subject to Edison's policies on personal dealing and conflicts of interest.

Copyright: Copyright 2019 Edison Investment Research Limited (Edison). All rights reserved FTSE International Limited (“FTSE”) © FTSE 2019. “FTSE®” is a trade mark of the London Stock Exchange Group companies and is used by FTSE International Limited under license. All rights in the FTSE indices and/or FTSE ratings vest in FTSE and/or its licensors. Neither FTSE nor its licensors accept any liability for any errors or omissions in the FTSE indices and/or FTSE ratings or underlying data. No further distribution of FTSE Data is permitted without FTSE’s express written consent.

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New Zealand

The research in this document is intended for New Zealand resident professional financial advisers or brokers (for use in their roles as financial advisers or brokers) and habitual investors who are “wholesale clients” for the purpose of the Financial Advisers Act 2008 (FAA) (as described in sections 5(c) (1)(a), (b) and (c) of the FAA). This is not a solicitation or inducement to buy, sell, subscribe, or underwrite any securities mentioned or in the topic of this document. For the purpose of the FAA, the content of this report is of a general nature, is intended as a source of general information only and is not intended to constitute a recommendation or opinion in relation to acquiring or disposing (including refraining from acquiring or disposing) of securities. The distribution of this document is not a “personalised service” and, to the extent that it contains any financial advice, is intended only as a “class service” provided by Edison within the meaning of the FAA (i.e. without taking into account the particular financial situation or goals of any person). As such, it should not be relied upon in making an investment decision.

United Kingdom

Neither this document and associated email (together, the "Communication") constitutes or form part of any offer for sale or subscription of, or solicitation of any offer to buy or subscribe for, any securities, nor shall it or any part of it form the basis of, or be relied on in connection with, any contract or commitment whatsoever. Any decision to purchase shares in the Company in the proposed placing should be made solely on the basis of the information to be contained in the admission document to be published in connection therewith.

This Communication is being distributed in the United Kingdom and is directed only at (i) persons having professional experience in matters relating to investments, i.e. investment professionals within the meaning of Article 19(5) of the Financial Services and Markets Act 2000 (Financial Promotion) Order 2005, as amended (the "FPO") (ii) high net-worth companies, unincorporated associations or other bodies within the meaning of Article 49 of the FPO and (iii) persons to whom it is otherwise lawful to distribute it. The investment or investment activity to which this document relates is available only to such persons. It is not intended that this document be distributed or passed on, directly or indirectly, to any other class of persons and in any event and under no circumstances should persons of any other description rely on or act upon the contents of this document (nor will such persons be able to purchase shares in the placing).

This Communication is being supplied to you solely for your information and may not be reproduced by, further distributed to or published in whole or in part by, any other person.

United States

The Investment Research is a publication distributed in the United States by Edison Investment Research, Inc. Edison Investment Research, Inc. is registered as an investment adviser with the Securities and Exchange Commission. Edison relies upon the "publishers' exclusion" from the definition of investment adviser under Section 202(a) (11) of the Investment Advisers Act of 1940 and corresponding state securities laws. This report is a bona fide publication of general and regular circulation offering impersonal investment-related advice, not tailored to a specific investment portfolio or the needs of current and/or prospective subscribers. As such, Edison does not offer or provide personal advice and the research provided is for informational purposes only. No mention of a particular security in this report constitutes a recommendation to buy, sell or hold that or any security, or that any particular security, portfolio of securities, transaction or investment strategy is suitable for any specific person.

Frankfurt +49 (0)69 78 8076 960

Schumannstrasse 34b

60325 Frankfurt

Germany

London +44 (0)20 3077 5700

280 High Holborn

London, WC1V 7EE

United Kingdom

New York +1 646 653 7026

1,185 Avenue of the Americas

3rd Floor, New York, NY 10036

United States of America

Sydney +61 (0)2 8249 8342

Level 4, Office 1205

95 Pitt Street, Sydney

NSW 2000, Australia

Frankfurt +49 (0)69 78 8076 960

Schumannstrasse 34b

60325 Frankfurt

Germany

London +44 (0)20 3077 5700

280 High Holborn

London, WC1V 7EE

United Kingdom

New York +1 646 653 7026

1,185 Avenue of the Americas

3rd Floor, New York, NY 10036

United States of America

Sydney +61 (0)2 8249 8342

Level 4, Office 1205

95 Pitt Street, Sydney

NSW 2000, Australia

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