Hutchison China MediTech — Surufatinib NETs solid data at ESMO

HCM continues to make rapid progress towards its goal of becoming an international biotech company with a marketed portfolio of innovative drugs. Of its late-stage pipeline, surufatinib, savolitinib and fruquintinib are in pole position to ensure HCM’s goal is reached in the medium term. Surufatinib has made significant strides this year; the Phase III SANET-ep trial cessation one year ahead of schedule due to overwhelming positive efficacy in advanced stage non-pancreatic NET means the drug could launch in China in late 2020. If the global Phase III trial (US and Europe due to initiate in H1 20) results are consistent with data seen in Chinese patients to date, this would pave the way for surufatinib to be the first universal small molecule drug treatment for NET.

Data from Frost & Sullivan indicate the global NET market in 2018 was worth approximately $5.8bn and is expected to grow to $21.2bn by 2030. NET cancers arise out of cells of the endocrine and nervous systems, predominately the digestive and respiratory tracts. NETs can be aggressive or indolent in nature, the latter meaning that patients can survive longer in the course of disease than certain solid tumors. NETs are typically classified as pancreatic NETs or extra pancreatic NETs (a catch all for a tumor that does not arise out the pancreas) and commonly include lung NETs and gastrointestinal (GI) NETs. NETs can be functional (~40% of patients) or non-functional depending on whether the hormones produced by the tumor lead to symptoms (functional NET).

In China there is significant market opportunity with reported incidence of NET in 2018 of approximately 67,600. While the current prevalence of NET in the US is ~150,000 patients (incidence of ~19,000 new cases per year), current treatment modalities are typically limited to subsets of NET with only Afinitor approved for a broad range of NETs (pancreatic, GI and lung).

Surufatinib’s China Phase III program consists of two studies evaluating the drug (vs placebo) in pancreatic NET (SANET-p, planned n=195) and non-pancreatic NET (SANET-ep, actual n=198), thus covering all NET patient types. In June 2019, HCM announced the independent data monitoring committee had recommended stopping the Phase III SANET-ep early following positive interim data. This was based on the trial meeting its primary endpoint of PFS and the trial was unblinded a year ahead of schedule. Upon unblinding, patients on placebo had the opportunity to cross over to the surufatinib arm. Surufatinib met primary endpoints and significantly improved investigator-assessed PFS (PFS 9.2 months vs placebo 3.8 months, HR=0.334, p<0.0001), and all secondary endpoints were additionally met vs placebo arm (ORR 10.3% vs 0%, p=0.005; DCR 86.5% vs 65.6%, p=0.002).

Eligibility criteria for the study included well differentiated extrapancreatic (ep) NET pathological grade 1 or 2 with advanced disease, patients with prior use of VEGF/VEGFR inhibitors were excluded. Around 69% of patients on surufatinib had received prior systemic anti-tumor therapy (chemotherapy, somatostatin analogues, everolimus) vs 64% on placebo.

Safety was in line with previous data; hypertension (64.3% on drug vs 26.5% on placebo) and proteinuria (70.5% on drug vs 52.9% on placebo), while the most common adverse events were medically manageable. Given surufatinib inhibits three different targets (vascular endothelial growth factors, VEGFRs; fibroblast growth factor receptor 1, FGFR1; and colony stimulating factor 1 receptor, CSF-1R) at therapeutic dosing; its tolerability with combination therapies is an important factor. However, median exposure days on surufatinib (217 days) and placebo (146 days) suggests discontinuation rates were largely due to disease progression rather than tolerability issues.

At ESMO 2019 HCM reported preliminary results of the global Phase Ib study of surufatinib in US solid tumor patients – HCM initiated the US Phase Ib/II study in P-NET and BTC in July 2018. The two-part study design including dose escalation and dose expansion assessed safety and tolerability. It confirmed a safety and PK (pharmacokinetic) profile consistent with studies in China patients. Importantly, surufatinib showed early signs of utility (two partial responses, n=15 pNET patients) in heavily pre-treated patients with some receiving up to eight different lines of therapy. The maximum tolerated dose/recommended Phase II dose was established as 300mg daily for global development.

HCM is building its China oncology commercial team ahead of surufatinib launch, with the intention to have full coverage of China in preparation for launch late 2020. NET will be surufatinib’s first (potential) approved indication. Non-pancreatic NET is estimated by HCM to represent ~80% of NET cases in China. SANET-p Phase III data (pancreatic NET H1 20) is critical to widening its market potential to an additional 10–20% of patients. Based on the SANET-ep data, of the Chinese patients with advanced disease, prior to enrolment around 40% had received treatment with chemotherapy, 30% with a somatostatin analogue and c 10% with everolimus; on the strength of the data presented we believe that surufatinib could provide a universal treatment for NET, particularly if SANET-p provides a similar benefit to patients with pancreatic NET (reduction in risk of disease progression). Pricing strategies in China will be important given competitor NRDL reference pricing of $2,007 per month for Sutent and $1,320 per month for Affinitor.

HCM plans to investigate surufatinib in other solid tumors both as monotherapy and in combination therapy with a PD-1 focus. HCM has multiple PD-1 collaborations in place; the Tuoyi (Junshi collaboration) dose expansion study in multiple tumor types is anticipated to start in Q419.

Following encouraging proof of concept data from the Phase II study in BTC, a pivotal open-label Phase IIb/III trial (NCT03873532) in China initiated in 2019. Interim data on the first 80 patients recruited into this trial are expected mid-2020. BTC represents a high unmet need due to limited treatment options and an increasing patient population.

Surufatinib’s global registration clinical trial is in planning stage. The end of Phase II meeting with the FDA is expected in Q419, with US and Europe Phase II/III estimated to start in H1 20.

To date no targeted therapies have been approved across the broad NET population. Although progress has been made in the treatment of NETs, most approved treatments are for subsets of NET, dependent on the primary site of NET, stage and grade. Treatment options include surgery where possible and long-term systemic treatment to treat symptoms and suppress tumor growth include somatostatin inhibitors such as Novartis’s Sandostatin LAR (octreotide) and Lutathera (177Lu-Affinitor), which slow the hormonal production driving the formation of NETs (ex lung). Approved drugs include somatostatin inhibitors, Afinitor, an mTOR inhibitor, and sunitinib, a tyrosine kinase inhibitor. Exhibit 2 highlights the different treatment options by NET subtype available in the US. In China, the Afinitor label has now been expanded to include the same NET indications as its USA label (pancreatic, GI and lung).

The treatment landscape is fragmented, for example Lanreotide data (CLARINET) supports use in pNET, and GI NET, while Sutent (sunitinib) data support its use in pNET only. Targeting aberrant angiogenic VEGF signalling has been proven with Sutent in treating pancreatic NETs, demonstrating a 5.9-month improvement in mPFS vs placebo (HR=0.42; p<0.001). However, Phase III efficacy for VEGFR inhibitors in treating extra-pancreatic NETs had not been established until SANET-ep. These data could establish surufatinib as a leading treatment option. Everolimus (Afinitor) has the broadest US label to date and is approved for pNET, and non-functional NET of lung or GI primary site of origin (full US prescribing label). This is based on data from the Phase III RADIANT4 trial. Afinitor is not approved for functional non-pancreatic NET. In China Afinitor is now approved for the same broad range of NETs as in the US (pancreatic, GI and lung). A limitation of Afinitor is that as an immunosuppressive agent, as such patients have increased risk of localized and systemic infections including pneumonia, bacterial, viral and fungal inhibitions of a severe or fatal nature. In its registrational study in patients with pNET tumors of a GI or lung origin, Afinitor was discontinued for adverse reactions in 29% of patients and dose reduction or delay was required in 70% of everolimus-treated patients. Serious adverse reactions occurred in 42% of everolimus-treated patients and included three fatal events (cardiac failure, respiratory failure and septic shock). Surufatinib Phase II data supported its broad spectrum efficacy in NET including Sutent/Afinitor failures; it is likely that the three-pronged target inhibition is its differentiating factor in patients who have progressed with these latter drugs.

Surufatinib is an oral angio-immunokinase inhibitor that targets VEGF1, 2 and 3; FGFR1 and CSF-1R kinases. During the last decade modalities of cancer treatment that involve targeted therapy (addressing cancer specific mutations), harnessing the power of the immune system and cancer cell blood supply to treat the tumor microenvironment are additional armaments to traditional chemotherapy and surgical treatment options. As such combination therapies evaluating drugs with multiple mechanism of action are approved (eg EGFR inhibitor plus PD-1 inhibition) or undergoing late-stage testing in a multitude of cancer. Surufatinib is a small molecule therapeutic protein that addresses three distinct kinases and thus multiple different regulatory processes that enable cancer proliferation:

Surufatinib’s three-in-one profile bodes well for current and evolving treatment paradigms in oncology where immunomodulatory drugs such as checkpoint inhibitors are being used in earlier lines of therapy.

We value HCM at $5.7bn ($42.78/ADS) vs $5.7bn ($42.62/ADS) previously. We now forecast surufatinib is launched in China in late 2020 (previously early 2021). We have increased 2020 R&D expenses and rolled our model forward in time. We use a risk-adjusted net present value (NPV) method to discount future cash flows for the innovation platform (savolitinib, fruquintinib, surufatinib, epitinib, HMPL-523 and HMPL-689) (valuation of $4,131.4m). We use earnings-based multiples for HCM’s commercial platform (subsidiaries and JVs). Applying a 20.4x multiple on our forecast 2019 net attributable profit (equity in earnings of equity investees, net of tax) for the JVs of $39.2m yields a valuation of $800.4m (Exhibit 3).

In June 2019, major shareholder CKHH completed an offering of some of its ADSs, which reduced its holding in HCM to 51.15% (from 60.2% previously). CKHH recently announced it had reduced its holding by 1.3% to below 50% (49.9%). This will enable CKHH to deconsolidate HCM from its accounts. CKHH remains committed to its investment in HCM and has no plans in the near future to reduce its holdings further. We see this as a positive for HCM as it removes a significant overhang on the shares. We note that this latest offering has had no effect on the number of shares in issue and does not dilute any current shareholders.