IMG-007 is under clinical development by Inmagene Biopharmaceuticals and currently in Phase II for Alopecia Areata. According to GlobalData, Phase II drugs for Alopecia Areata have a 48% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how IMG-007’s drug-specific PTSR and Likelihood of Approval (LoA) scores compare to the indication benchmarks. Buy the report here.
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GlobalData tracks drug-specific phase transition and likelihood of approval scores, in addition to indication benchmarks based off 18 years of historical drug development data. Attributes of the drug, company and its clinical trials play a fundamental role in drug-specific PTSR and likelihood of approval.
IMG-007 overview
IMG-007 is under development for the treatment of atopic dermatitis and alopecia areata. The therapeutic candidate acts by targeting OX40. It is administered through intravenous and subcutaneous route. It is being developed based on QuadraTek platform
It was also under development for graft versus host disease, asthma, rheumatoid arthritis and inflammatory bowel disease.
Inmagene Biopharmaceuticals overview
Inmagene Biopharmaceuticals (Inmagene) is a clinical-stage biotechnology company that develops novel therapeutics for immunological and inflammatory diseases using the QuadraTek platform. The company’s pipeline candidates include IMG-007, IMG-008, IMG-004 and IMG-020 (izokibep) and IMG-018. Its pipeline candidates treat atopic dermatitis, alopecia areata, rheumatoid arthritis (RA), chronic spontaneous urticaria (CSU), generalized pustular psoriasis (GPP), hidradenitis suppurativa (HS), psoriatic arthritis (PsA), hidradenitis suppurativa (HS), uveitis psoriasis and ankylosing spondylitis. The company works in partnership with pharmaceutical and biotechnology companies such as Hutchmed and Affibody AB. ChiInmagene is headquartered in San Diego, California, the US.
For a complete picture of IMG-007’s drug-specific PTSR and LoA scores, buy the report here.
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GlobalData, the leading provider of industry intelligence, provided the underlying data, research, and analysis used to produce this article.
GlobalData’s Likelihood of Approval analytics tool dynamically assesses and predicts how likely a drug will move to the next stage in clinical development (PTSR), as well as how likely the drug will be approved (LoA). This is based on a combination of machine learning and a proprietary algorithm to process data points from various databases found on GlobalData’s Pharmaceutical Intelligence Center.
