Excellent end to the year

Cantargia 17 December 2019 Update
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Cantargia

Excellent end to the year

Company update

Pharma & biotech

17 December 2019

Price

SEK19.9

Market cap

SEK1.45bn

Net cash (SEKm) at end-Q319 (includes short-term investments)

194.5

Shares in issue

72.8m

Free float

90%

Code

CANT

Primary exchange

Nasdaq Stockholm

Secondary exchange

N/A

Share price performance

%

1m

3m

12m

Abs

30.1

24.1

24.4

Rel (local)

26.8

14.5

(0.2)

52-week high/low

SEK21.6

SEK12.8

Business description

Cantargia is a clinical-stage biotechnology company based in Sweden, established in 2009 and listed on the Nasdaq Stockholm main market. It is developing two assets against IL1RAP, CAN04 and CAN10. CAN04 is being studied in a Phase IIa clinical trial, CANFOUR, in solid tumours focusing on NSCLC and pancreatic cancer. Cantargia is preparing to file an IND and initiate a trial in the US next year.

Next events

Initiate new US study with CAN04 in combination with CPIs

H120

Phase IIa CANFOUR updates

2020

CAN10 preclinical development updates

2020

Analyst

Jonas Peciulis

+44 (0)20 3077 5728

Cantargia is a research client of Edison Investment Research Limited

Over the past several weeks Cantargia has reported positive interim data from the ongoing Phase IIa trial with lead asset CAN04, an anti-IL1RAP antibody targeting the IL-1 pathway, announced the first clinical trial in the US and introduced CAN10, a preclinical project in inflammation uniquely targeting three interleukin pathways, IL-1, IL-33 and IL-36. Two days after the introduction of CAN10, J&J’s Janssen announced the acquisition of bermekimab from the US-based XBiotech for an impressive $750m upfront and $600m in potential milestones. The mechanism of action of bermekimab, which is in mid-stage clinical trials as an anti-inflammatory anti-IL-1-alpha antibody, partially overlaps with that of CAN10. Our Cantargia valuation is SEK2.94bn or SEK40.4/share (virtually unchanged).

Year end

Revenue (SEKm)

PBT*
(SEKm)

EPS*
(SEK)

DPS
(SEK)

P/E
(x)

Yield
(%)

12/17

0.0

(60.3)

(1.86)

0.0

N/A

N/A

12/18

0.0

(91.2)

(1.38)

0.0

N/A

N/A

12/19e

0.0

(100.7)

(1.45)

0.0

N/A

N/A

12/20e

0.0

(114.1)

(1.57)

0.0

N/A

N/A

Note: *PBT and EPS are normalised, excluding amortisation of acquired intangibles, exceptional items and share-based payments.

Phase IIa CANFOUR data

On 2 December 2019, Cantargia reported interim data from the ongoing open-label, three-arm Phase IIa study with CAN04 in combination with first-line, standard of care (SoC) chemotherapy in non-small cell lung cancer (NSCLC) and metastatic pancreatic cancer (pancreatic ductal adenocarcinoma, PDAC). Four of seven evaluable patients with PDAC achieved partial response (PR) and two out of three evaluable patients with NSCLC achieved an objective response (OR); there was one complete response (CR) and one PR. Although the data are early, the results compare favourably to response rates to standalone chemotherapy regimens used in the CANFOUR trial (23% in PDAC; 22–28% in first-line NSCLC). These results support the hypothesis that CAN04 is synergistic with the SoC chemotherapy.

US study to test CAN04 combo with CPIs

The recruitment to the PDAC and NSCLC arms is expected to be completed in early Q220 and Q320, respectively, with key survival results due in 2021. The somewhat slower than expected enrolment to the NSCLC arm was addressed by opening additional centres. Cantargia recently announced a major expansion of its clinical programme with plans to initiate a Phase Ib study in the US. The company will file for an investigational new drug (IND) application in January and the trial could start in H120. The trial design is yet to be confirmed, but the goal is to explore the potential of CAN04 combination with checkpoint inhibitors (CPIs) in three indications (NSCLC, head and neck cancer and bladder cancer).

Valuation: SEK2.94bn or SEK40.4/share

Our valuation of Cantargia is virtually unchanged at SEK2.94bn or SEK40.4/share versus SEK2.65bn or SEK36.4/share previously. Updates on recruitment progress for the Phase IIa CANFOUR trial and the initiation of the US study are the most visible R&D events in the near term.

Interim data from the Phase IIa CANFOUR trial

On 2 December 2019, Cantargia reported interim data from the ongoing open-label, three-arm Phase IIa study with CAN04 in NSCLC and PC as monotherapy and in combination with first-line chemotherapies (Exhibit 2). The CANFOUR trial consists of two parts – Phase I and Phase IIa. The full Phase I data were presented at ASCO on 2 June 2019, which showed that CAN04 was generally safe and well tolerated. The ongoing Phase IIa study includes initial efficacy endpoints among others. The first results include:

No major new side effects were reported.

Two out of three evaluable patients with metastatic NSCLC achieved ORs (there was one CR and one PR).

Four out of seven evaluable patients with metastatic pancreatic cancer (PDAC) achieved PR:

Of these four patients, three had more than a 90% decrease in CA19-9, which is a biomarker for pancreatic cancer tumour burden.

The remaining three patients had a progressive disease; however, one of those three patients showed pseudoprogression and a pronounced decrease in the CA19-9 biomarker.

The results showed the addition of CAN04 increased the response to treatment rates compared to historical efficacy rates of the same standard of care chemotherapy regimens. Reported historical response rates with the chemotherapy regimens used in the CANFOUR trial are 23% (PDAC; Von Hoff et al, 2013), 22–28% in first-line NSCLC (Schiller et al, 2002; Scagliotti et al, 2008). Also, the historical data showed more than a 90% reduction of CA19-9 was reported in 31% of PDAC patients after standard gemcitabine/abraxane therapy (Von Hoff et al, 2013).

Moreover, the pseudoprogression case is particularly interesting because it is a known phenomenon when treating patients with immunotherapies. It is defined as ‘a response to treatment after initial increase in volume of cancer lesions, due to the infiltration of tumoral tissue by immune cells’. Although the patient was still considered to have progressive disease during the last check, the pseudoprogression phenomenon after the administration of CAN04 would imply the immune system was activated. This is supportive to the expected mechanism of action of CAN04. In addition to direct cell killing via antibody-dependent cellular cytotoxicity, by inhibiting IL1RAP CAN04 blocks the IL-1 signalling pathway, which the tumour exploits as a defence strategy against immune system attack.

Overall, although the data are still at an early stage, the large margin in achieved ORs compared to historical controls provides some confidence in the hypothesis that CAN04 is synergistic with the SoC chemotherapy.

Next steps

The recruitment to the PDAC arm is expected to be completed in early Q220. Cantargia reported somewhat slower than expected enrolment to the NSCLC arm. To address that, the company opened additional centres and recruitment is expected to be completed in early Q320. More response, biomarker and safety data will likely be released in 2020. In addition to the chemotherapy combination, the Phase IIa CANFOUR trial includes a monotherapy arm primarily analysing safety and biomarkers in patients with late-stage disease with results from different dose levels expected in H120. The key readouts (progression free survival and overall survival) from the combination arms are likely in 2021.

Exhibit 1: Phase IIa CANFOUR trial interim data

Source: Cantargia

Exhibit 2: Phase IIa CANFOUR trial design

Source: Cantargia

Clinical development expansion in the US

On 15 November 2019, Cantargia announced it is proceeding with plans to initiate a clinical trial in the US, which followed a positive pre-IND meeting with the FDA. Cantargia plans to file for the IND application in January 2020. The rationale to test CAN04 in combination with CPIs is based on several observations:

Myeloid suppressive cells, such as tumour associated macrophages or myeloid derived suppressor cells, express IL1RAP and play a substantial role in PD-1 resistance.

IL-1 upregulates PD-L1 on macrophages and induces downstream factors, such as IL-6, which add to immunosuppression in the tumour microenvironment.

IL-1beta blockade has been shown to reverse the tolerance to anti-PD-1 in an in vivo setting.

The trial design has not yet been confirmed, but preliminary to this will be a Phase Ib trial with CAN04 in combination with checkpoint inhibitors in three indications: NSCLC, head and neck squamous cancer (HNSC) and bladder cancer. These indications were selected because the tumours express IL1RAP and are relatively immunogenic, therefore suitable for treatment with CPIs. In addition, checkpoint inhibitor (Keytruda) is a standard therapy in these indications. The patients in the trial will be eligible if they have progressed on prior PD1/PDL-1 antibody therapy. (second-line positioning). Up to 18 patients are planned to be included in the trial. Endpoints will include typical safety evaluation, as well as exploratory biomarkers and initial efficacy. The trial could start in Q220.

CAN10: New preclinical project introduced

In addition to its lead project CAN04, Cantargia and its collaborator Panorama Research worked together on the preclinical programme CANxx. CANxx is focused on the discovery of an antibody against IL1RAP that has the potential to treat autoimmune and inflammatory diseases with the involvement of three interleukin pathways (IL-1, IL-33 and IL-36). On 5 December 2019, Cantargia announced it had selected CAN10 for preclinical development. The project includes two different antibodies that show potential in targeting all three pathways. Cantargia expects to name the drug candidate later and, in case of favourable results, the Phase I trial could start in 2021.

Exhibit 3: CAN10 simultaneously targets IL-1, IL-33 and IL-36 pathways

Source: Cantargia

Exhibit 4: CAN10 reduces inflammation in animal disease model

Source: Cantargia

Based on an extensive literature review Cantargia selected two indications on which to focus: systemic sclerosis and myocarditis. The rationale for selecting these indications is that all three interleukin pathways are involved. Both conditions can be described as orphan indications, so Cantargia could develop these projects on its own. In contrast, CAN10’s mechanism of action makes it a unique asset and we do not know of any other R&D projects in development that simultaneously target the three interleukins. From the perspective of competition, this makes it a potentially attractive in-licensing target for pharma companies in the anti-inflammatory drug development field.

To this end, US-based XBiotech announced on 7 December 2019 that Janssen (Johnson & Johnson) acquired its anti-IL-1alpha antibody bermekimab for $750m upfront and $600m in potential milestones payments. Initially, XBiotech tested bermekimab in oncology; however, results from Phase III trials in colorectal cancer were mixed and ultimately the antibody was repositioned for inflammatory diseases. XBiotech is running two mid-stage clinical trials with bermekimab for hidradenitis suppurativa and atopic dermatitis, but the company will be prohibited (for anti-competitive reasons) from entering dermatology again with new antibodies, presumably the area of interest for Janssen. Although it is still not clear what Janssen’s plans with bermekimab are, the deal terms suggest its interest in this pathway is very high.

Given its troubled past in oncology, the comeback that XBiotech has made in dermatology is remarkable. With CAN04 Cantargia does not target inflammatory diseases, but CAN10’s mechanism of action does overlap that of bermekimab. Theoretically, as we described in our initiation report, anti-IL1RAP antibodies (CAN10 and CAN04) would have a more profound downstream effect as they block the signalling via both IL-1alpha and IL-1beta receptors, as opposed to inhibiting only IL-1alpha (eg bermekimab) or IL-1beta (eg canakinumab, Novartis).

Another deal involving interleukin-based assets was announced on 9 December 2019, when Sanofi agreed to pay $2.5bn for Synthorx, a biotech company in California, US. Synthorx’s lead compound is THOR-707, a variant of IL-2. To our knowledge, there is no significant overlap between the downstream effects of IL-2 and the three interleukin pathways Cantargia is targeting (IL-1, IL-33 and IL-36). Therefore, this deal is not directly comparable. However, when taken together the XBiotech and Synthorx deals demonstrate pharma’s interest in immunotherapies exploiting interleukin pathways.

Financials and valuation

With its Q319 results, Cantargia reported an operating loss of SEK26.3m versus SEK21.4m in Q318. R&D costs in Q219 were SEK23.2m versus SEK16.7m in Q318, an increase due to the initiation of the larger Part 2 (Phase IIa) of the CANFOUR trial. We have adjusted our operating loss slightly to SEK101.1m and SEK114.1m for 2019 and 2020, from SEK94.9m and SEK117.8m, respectively. The reported cash position at end Q319 was SEK194.5m (including short-term investments).

Our updated valuation of Cantargia is higher at SEK2.94bn or SEK40.4/share versus SEK2.65bn or SEK36.4/share previously, as we slightly increased the success probability for CAN04 to reach the market to 18% from 15% to reflect the early positive interim data. The modest revision of our estimates and rolling our model forward were offset by the lower cash position. Potential catalysts for Cantargia’s share price in the near term include:

The initiation of the US trial with CAN04 in combinations with checkpoint inhibitors (likely Q220);

Phase IIa CANFOUR trial combination results in PDAC and NSCLC:

more response, biomarker and safety data in 2020;

progression free survival and overall survival in 2021;

Phase IIa CANFOUR trial monotherapy biomarker/biopsy results (2020); and

CAN10 preclinical development update.

Exhibit 5: Sum-of-the-parts Cantargia valuation

Product

Launch

Peak sales
($m)

Unrisked NPV (SEKm)

Unrisked NPV/
share (SEK)

Technology probability (%)

rNPV
(SEKm)

rNPV/share (SEK)

CAN04 – NSCLC

2026

3,100

6,518.6

89.5

18.0%

1,186.6

16.3

CAN04 – pancreatic cancer

2024

2,100

6,614.9

90.9

18.0%

1,587.9

21.8

Net cash/short-term investments, FY19e

165.3

2.3

100%

165.3

2.3

Valuation

13,298.8

182.7

 

2,939.8

40.4

Source: Edison Investment Research. Note: WACC = 12.5% for product valuations.

Exhibit 6: Financial summary

SEK000s

2017

2018

2019e

2020e

Year end 31 December

IFRS

IFRS

IFRS

IFRS

PROFIT & LOSS

Revenue

 

 

0

0

0

0

Cost of Sales

0

0

0

0

Gross Profit

0

0

0

0

Research and development

(52,419)

(76,951)

(86,951)

(99,602)

EBITDA

 

 

(60,010)

(93,306)

(101,074)

(114,149)

Operating Profit (before amort. and except.)

 

 

(60,010)

(93,306)

(101,074)

(114,149)

Intangible Amortisation

0

0

0

0

Exceptionals

0

0

0

0

Other

0

0

0

0

Operating Profit

(60,010)

(93,306)

(101,074)

(114,149)

Net Interest

(243)

2,145

360

0

Profit Before Tax (norm)

 

 

(60,253)

(91,161)

(100,715)

(114,149)

Profit Before Tax (reported)

 

 

(60,253)

(91,161)

(100,715)

(114,149)

Tax

0

0

0

0

Profit After Tax (norm)

(60,253)

(91,161)

(100,715)

(114,149)

Profit After Tax (reported)

(60,253)

(91,161)

(100,715)

(114,149)

Average Number of Shares Outstanding (m)

32.4

66.2

69.5

72.8

EPS - normalised (SEK)

 

 

(1.86)

(1.38)

(1.45)

(1.57)

Dividend per share (SEK)

0.0

0.0

0.0

0.0

Gross Margin (%)

N/A

N/A

N/A

N/A

EBITDA Margin (%)

N/A

N/A

N/A

N/A

Operating Margin (before GW and except.) (%)

N/A

N/A

N/A

N/A

BALANCE SHEET

Fixed Assets

 

 

2,957

2,957

2,957

2,957

Intangible Assets

0

0

0

0

Tangible Assets

0

0

0

0

Investments

2,957

2,957

2,957

2,957

Current Assets

 

 

271,496

168,486

184,426

70,277

Stocks

0

0

0

0

Debtors

0

0

0

0

Cash

149,781

76,528

25,283

51,134

Other*

121,715

91,958

159,143

19,143

Current Liabilities

 

 

(28,334)

(16,398)

(35,014)

(35,014)

Creditors

(28,334)

(16,398)

(35,014)

(35,014)

Short term borrowings

0

0

0

0

Long Term Liabilities

 

 

0

0

0

0

Long term borrowings

0

0

0

0

Other long term liabilities

0

0

0

0

Net Assets

 

 

246,119

155,045

152,369

38,220

CASH FLOW

Operating Cash Flow

 

 

(40,860)

(105,165)

(99,962)

(114,149)

Net Interest

(243)

478

360

0

Tax

0

0

0

0

Capex

0

0

0

0

Acquisitions/disposals

0

0

0

0

Financing

304,479

0

98,037

0

Other*

(139,499)

31,434

(49,680)

140,000

Dividends

0

0

0

0

Net Cash Flow

123,877

(73,253)

(51,245)

25,851

Opening net debt/(cash)

 

 

(25,904)

(149,781)

(76,528)

(25,283)

HP finance leases initiated

0

0

0

0

Other

0

0

0

(0)

Closing net debt/(cash)

 

 

(149,781)

(76,528)

(25,283)

(51,134)

Source: Cantargia accounts, Edison Investment Research. Note: *Mainly short-term investments.


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This report has been commissioned by Cantargia and prepared and issued by Edison, in consideration of a fee payable by Cantargia. 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 research department of Edison 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.

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Schumannstrasse 34b

60325 Frankfurt

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London, WC1V 7EE

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1,185 Avenue of the Americas

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United States of America

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Level 4, Office 1205

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General disclaimer and copyright

This report has been commissioned by Cantargia and prepared and issued by Edison, in consideration of a fee payable by Cantargia. 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 research department of Edison 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.

Australia

Edison Investment Research Pty Ltd (Edison AU) is the Australian subsidiary of Edison. Edison AU is a Corporate Authorised Representative (1252501) of Crown Wealth Group Pty Ltd who holds an Australian Financial Services Licence (Number: 494274). This research is issued in Australia by Edison AU and any access to it, is intended only for "wholesale clients" within the meaning of the Corporations Act 2001 of Australia. Any advice given by Edison AU is general advice only and does not take into account your personal circumstances, needs or objectives. You should, before acting on this advice, consider the appropriateness of the advice, having regard to your objectives, financial situation and needs. If our advice relates to the acquisition, or possible acquisition, of a particular financial product you should read any relevant Product Disclosure Statement or like instrument.

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

This document is prepared and provided by Edison for information purposes only and should not be construed as an offer or solicitation for investment in any securities mentioned or in the topic of this document. A marketing communication under FCA Rules, this document has not been prepared in accordance with the legal requirements designed to promote the independence of investment research and is not subject to any prohibition on dealing ahead of the dissemination of investment research.

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.

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

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.

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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

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