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'Still The Place To Do Drug Innovation': China Biotech CEO Podcast With InnoCare’s Jasmine Cui

R&D Speed, New Drug Coverage, Biogene, Incyte partnerships

Executive Summary

From founding to the approval and commercial launch of its first innovative drug took Beijing-based biotech InnoCare just seven years. After a listing in Hong Kong, the firm is now heading to Shanghai after obtaining the green light for a second listing from the STAR board.

(This is the third instalment in a new China Biotech CEO Podcast series, in which top executives sit down to discuss key issues impacting innovative drug development in China, potentially the largest pharma market in the world. The first episode was with CANbridge Pharmaceuticals Inc.CEO James Xue (Also see "China Biotech CEO Podcast: CANbridge’s Xue On Orphan Drug Coverage, Financing, Gene Therapy" - Scrip, 27 Apr, 2022.) and the second with Jiangsu Hengrui Medicine Co., Ltd.'s US subsidiary Luzsana's CEO Scott Filosi and CMO Joseph Eid. (Also see "CEO Podcast: Hengrui's US Subsidiary's CEO, CMO On Chinese Pharma Going Global" - Scrip, 8 Jun, 2022.))

In this hour-long, sit-down interview with Scrip, InnoCare Pharma Ltd. co-founder and CEO Jasmine Cui discusses how the company leveraged timing, a lead asset and domestic regulatory reforms to its advantage to move from a startup to a clinical and commercial stage biotech in a short period of time.

In particular, regulatory changes initiated in 2017 and reimbursement for innovative new drugs, initiated in 2018 despite steep price reductions, are seen as contributing to the firm's relatively rapid development.

During the interview, Cui says sales of InnoCare's only commercial asset orelabrunitib - approved for chronic lymphoma leukemia and small lymphoma leukemia - have been strong due to inclusion in China's national reimbursement list.

In the first year of market launch in 2021, sales were CNY200m ($29m) and revenues for the first half of 2022 have already exceeded that figure, despite a comparatively small sales force of 250.

Innocare CEO Jasmine Cui

(InnoCare CEO Jasmine Cui. Courtesy InnoCare)

Listed in Hong Kong in 2020, the Beijing-based biotech views its planned listing in Shanghai as a homecoming. Rooted in China, the second listing will give it increased access to mainland investors, better communication with Chinese investors and expanded access to potential local partners.

Partnerships have become increasingly important as the company eyes expansion to more indications beyond hematologic malignancies, solid tumors and autoimmune conditions. It has signed an agreement with Biogen, Inc. to develop its BTK inhibitor orelabrunitib for multiple sclerosis and with Incyte Corporation for the US biotech’s tafasitamab for diffuse large B-cell lymphoma. (Also see "Asia Deal Watch: Incyte Inks Chinese Marketing Partnership With InnoCare For Monjuvi" - Scrip, 18 Aug, 2021.)

However, more than two years since the COVID-19 pandemic, there is emerging "innovation fatigue" among Chinese drug makers, which in the past have largely devoted the bulk of their R&D resources to hotly-pursued and well-established targets such as anti-PD-1 antibodies. Facing an unprecedented funding crunch, this fatigue, called “Neijuan” and “Tangping” in Chinese, has become prevalent in the sector.

Adding to this is a changing China, where compared to just several years ago, the cost of drug development has soared substantially. Unlike in 2017, when cancer trial enrolment was completed on time, oncology drug developers are now racing each other to secure enough patients for their studies.

Cui said that, despite that, China remains "the place for drug innovation," advising that "you have to prepare well and understand the local needs, especially the patients' needs." On top of that, regulators at the Center for Drug Evaluation are “really open and listening now,” while Chinese physicians are also catching up with their overseas peers.

Rare diseases such as multiple sclerosis in particular still have a large unmet need in China, which still looms large in global drug development and remains "the place to be," Cui concluded.

 Timestamps:
  • 0000-0005: Opening. Introduction of InnoCare and CEO's professional background

  • 0005-0010: Listing in Hong Kong and lessons learned

  • 0010-0015: rationale for the Shanghai second listing and goals to achieve, liquidity of HK Stock Exchange for so-called 18A pre-revenue biotech companies

  • 0015-0020: factors behind the relatively rapid R&D for InnoCare in China. Factors contributing to the development and approval of China’s third BTK inhibitor orelabrutinib

  • 0020-0025: Innovative new drug evaluation in China: from expensive to more affordable, driven by domestic innovation and annual drug reimbursement

  • 0025-0030: Coverage for innovative drugs. National Reimbursement drug list and price negotiations. Lessons learned and striking a balance between price and access

  • 0035-0040: Differentiation amid sizzling competition in China for hotly-pursued antibody targets.

  • 0040-0045: Going global. Partnerships with Biogen and Incyte, who are considered partners of choice, drug development for Chinese biotechs in the US

  • 0045-0050: Why Chinese biotechs have seen setbacks in the US after FDA issued complete response letters to Chinese PD-1s

  • 0050-0055: China’s changing new drug development has seen harder patient enrolment, soaring costs and insufficient primary investigators. How to handle the new reality?

  • 0055-0058:30: What makes a female CEO in biotech and how to get there?

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