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IMMUNOLOGY MARKET ANALYSIS

Immunology Market, By Drug Class (Monoclonal Antibody (mAb), Fusion Proteins, Immunosuppressants, Polyclonal Antibody, Others), By Disease Indication (Rheumatoid Arthritis, Psoriatic Arthritis, Plaque Psoriasis, Ankylosing Spondylitis, Inflammatory Bowel Disease, Prophylaxis of Organ Rejection, Others), By Distribution Channel (Hospital Pharmacies, Retail Pharmacies, Online Pharmacies), By Geography (North America, Latin America, Europe, Asia Pacific, Middle East & Africa)

  • Published In : Jun 2024
  • Code : CMI4594
  • Pages :179
  • Formats :
      Excel and PDF
  • Industry : Pharmaceutical

Key Developments

  • On May 22, 2024, Biogen Inc, an American multinational biotechnology company, and Human Immunology Biosciences, a privately-held clinical-stage biotechnology firm specializing in tailored treatments for individuals with severe immune-mediated diseases (IMDs), announced that both companies had signed definitive agreement. According to the agreement, Biogen will purchase HI-Bio for an initial sum of US$ 1.15 billion, with the potential for additional milestone payments totaling up to US$ 650 million.
  • On May 15, 2024, Blackstone, a investment management company, introduced Uniquity Bio, a clinical-stage drug development company concentrating on immunology and inflammation, within the Blackstone Life Sciences (“Blackstone”) portfolio. Uniquity Bio emerges from secrecy with the FDA's approval of its Phase 2 investigational new drug (“IND”) application for solrikitug, a monoclonal antibody aimed at TSLP, and is set to receive up to US$300 million in funding from Blackstone to progress the asset across various indications.
  • In April 2023, Merck, recognized as MSD, a multinational science and technology company, and Prometheus Biosciences, Inc., a biopharmaceutical company, announced that both companies had signed a definitive agreement. According to this agreement, Merck, via a subsidiary, will purchase Prometheus for US$ 200.00 per share in cash.
  • In November 2022, Genmab, a biotech company, and BioNTech, a Germany-based biotechnology company, collaborated to develop the DuoBody-PD-L1x4-1BB (GEN1046) monoclonal antibody for Phase 1/2 trials in solid tumors and Phase 2 trials in non-small cell lung cancer
  • In October 2022, the U.S. FDA granted approval for the combination of durvalumab (Imfinzi) and tremelimumab (Imjudo) for individuals with unresectable hepatocellular carcinoma, the predominant form of liver cancer

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