Daily BriefsHealthcare

Daily Brief Health Care: Takeda Pharmaceutical, Sciclone Pharmaceuticals, Medlab Clinical and more

In today’s briefing:

  • Takeda Strengthens Oncology Portfolio with HUTCHMED’s Fruquintinib Acquisition
  • Sciclone Pharmaceuticals (6600.HK) – The Business, the Outlook and the Challenges
  • Medlab Clinical – NanaBis development centre stage in 2023

Takeda Strengthens Oncology Portfolio with HUTCHMED’s Fruquintinib Acquisition

By Shifara Samsudeen, ACMA, CGMA

  • Takeda announced Monday that it has entered into an exclusive licensing agreement with HUTCHMED (China) for further development and commercialisation of Fruquintinib outside of Mainland China, Macau and Hong Kong.
  • Takeda will pay HUTCHMED $400m upfront and up to $730m in additional potential payments relating to regulatory, development and commercial sales milestones, as well as royalties on net sales.
  • Fruquintinib was approved in China in 2018, is a highly selective, oral VEGFR1/2/3 Tyrosine Kinase Inhibitor and offers potential new treatment option for patients with refractory metastatic colorectal cancer (CRC).

Sciclone Pharmaceuticals (6600.HK) – The Business, the Outlook and the Challenges

By Xinyao (Criss) Wang

  • Zadaxin has been the biggest performance driver of SciClone, but it would face the risk of losing market share and increased pricing pressures after generic drugs were included in VBP.
  • SciClone is primarily a pharmaceutical development/sales company, rather than a research-based innovative drug company.The increasingly low cost performance of in-licensed products has made the capital “reconsider” and be more rational.
  • SciClone is a good stock for short-term trade, especially by taking advantage of the positive momentum after it reaches licensing deals/launches new products, but we’re concerned about its long-term prospects.

Medlab Clinical – NanaBis development centre stage in 2023

By Edison Investment Research

As Medlab Clinical moves into 2023, the expected commencement of a Phase III trial for NanaBis (the company’s cannabinoid based analgesic therapy) in cancer-induced bone pain will be the focus for investors. Management made considerable progress towards Phase III in 2022, by switching to a purely synthetic cannabinoid formulation and gathering encouraging real-world data on NanaBis use. We believe these actions should maximise the potential for NanaBis in both a regulatory and a commercial setting. We note that successful progression of the company’s programmes will be contingent on Medlab’s ability to raise capital, given the short cash runway (funded into March 2023) and recent setback with the Nasdaq listing plans. We update our estimates to reflect the financing risk and macro uncertainty, resulting in our valuation decreasing to A$183.5m or A$80.4/share, from A$236.1m or A$103.5/share.


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