Daily BriefsHealthcare

Daily Brief Health Care: WuXi XDC Cayman Inc, Mirxes Holding, Green Cross and more

In today’s briefing:

  • WuXi XDC Cayman Pre-IPO – The Positives – Sales Have Surged Leading to Market Share Gains
  • Pre-IPO Mirxes Holding Company – The Profit Model in the Post Pandemic Era Needs to Be Verified
  • Green Cross (006280 KS): Turns Profitable in Q2; All Eyes on the Maiden US Approval of Blood Product


WuXi XDC Cayman Pre-IPO – The Positives – Sales Have Surged Leading to Market Share Gains

By Clarence Chu

  • WuXi XDC Cayman Inc (1877628D HK) is looking to raise at least US$100m in its upcoming Hong Kong IPO.
  • WuXi XDC Cayman (WXDC) is a CRDMO focused on the global antibody drug conjugates (ADC) and broader bioconjugate market providing integrated and end-to-end services.
  • In this note, we will talk about the positive aspects of the deal.

Pre-IPO Mirxes Holding Company – The Profit Model in the Post Pandemic Era Needs to Be Verified

By Xinyao (Criss) Wang

  • Although Mirxes has already commercialized its products, its total revenue fluctuated greatly. When the market demand for COVID-19 testing kits sharply declined, the Company’s financial position deteriorated immediately.
  • With the highest incidence rate of gastric cancer worldwide, PRC market is important to Mirxes. How to gain recognition from doctors and enter hospital market is a challenge for GASTROClear.
  • Mirxes is facing survival problem and eager for an IPO. Before Mirxes establishes a clear/visible path to commercialization and a successful profit model in post-COVID era, we would remain cautious. 

Green Cross (006280 KS): Turns Profitable in Q2; All Eyes on the Maiden US Approval of Blood Product

By Tina Banerjee

  • Green Cross (006280 KS) reported decent Q2 performance, with revenue and operating profit increasing 2% and 81%, YoY, respectively. Vaccine and blood products business remained the major growth drivers.
  • The company has re-submitted marketing application for GC5107, a blood derivative product to the FDA, which has accepted it with a target action date of January 13, 2024.
  • If approved, the company aims to enter the U.S. market in 2H24. Supply shortage amid increasing demand makes the U.S. an attractive market for the company’s blood products.

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