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HUTCHMED (China) Limited >
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Innovative pipeline closer to realising its potential

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  • 11 Aug 2020

Innovative pipeline closer to realising its potential


HUTCHMED (China) Limited (HCM:LON) | 230 27.6 5.3% | Mkt Cap: 1,989m


  • Trinity Delta
    • Lala Gregorek

    • 11 pages

Pharmaceuticals image



 
Pharmaceuticals image



Hutchison China MediTech (Chi-Med) continues to gather momentum as its pipeline gets closer to unlocking its potential. Increased visibility for the three lead assets with multiple catalysts in the next 6 to 18 months suggest significant upside potential. In China, Chi-Med is leveraging its established base to build a fully integrated oncology business, with its c 320-strong China Oncology commercial team set to take over Elunate marketing from October and execute its first unpartnered China launch in Q420 assuming surufatinib approval. A ninth drug candidate discovered in-house (HMPL-306) has entered the clinic in China, while five assets are in development for global markets. The first FDA submission (surufatinib) should start before year-end, with fruquintinib and savolitinib in or approaching global registration trials. Our updated valuation is £5.87/share or $38.17/ADS.


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Innovative pipeline closer to realising its potential


HUTCHMED (China) Limited (HCM:LON) | 230 27.6 5.3% | Mkt Cap: 1,989m


  • Published: 11 Aug 2020
  • Author: Lala Gregorek
  • Pages: 11
  • Trinity Delta


Hutchison China MediTech (Chi-Med) continues to gather momentum as its pipeline gets closer to unlocking its potential. Increased visibility for the three lead assets with multiple catalysts in the next 6 to 18 months suggest significant upside potential. In China, Chi-Med is leveraging its established base to build a fully integrated oncology business, with its c 320-strong China Oncology commercial team set to take over Elunate marketing from October and execute its first unpartnered China launch in Q420 assuming surufatinib approval. A ninth drug candidate discovered in-house (HMPL-306) has entered the clinic in China, while five assets are in development for global markets. The first FDA submission (surufatinib) should start before year-end, with fruquintinib and savolitinib in or approaching global registration trials. Our updated valuation is £5.87/share or $38.17/ADS.



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