Rosnilimab is under clinical development by AnaptysBio and currently in Phase II for Rheumatoid Arthritis. According to GlobalData, Phase II drugs for Rheumatoid Arthritis have a 35% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how Rosnilimab’s drug-specific PTSR and Likelihood of Approval (LoA) scores compare to the indication benchmarks. Buy the report here.

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.

Rosnilimab overview

Rosnilimab (ANB-030) is under development for the treatment of ulcerative colitis and moderate-to-severe rheumatoid arthritis. It is administered by subcutaneous and intravenous route. The drug candidate acts by targeting PD-1 immune checkpoint. It is developed based on the somatic hypermutation (SHM) platform.
It was under development of alopecia areata, graft versus host disease, vitiligo and inflammatory diseases.

AnaptysBio overview

AnaptysBio (Anaptys) is a clinical-stage biotechnology company. It is focused on advancing immune cell-modulating antibodies for autoimmune and inflammatory diseases. The company’s product candidates include rosnilimab, a PD-1 agonist in trials for rheumatoid arthritis and ulcerative colitis, and ANB032, a BTLA agonist in development for atopic dermatitis. Its preclinical pipeline features ANB033, targeting CD122 to manage inflammation, and ANB101, a BDCA2 modulator to regulate dendritic cells. The company is also advancing cytokine antagonists imsidolimab, targeting IL-36R for generalized pustular psoriasis, and etokimab, an IL-33 antagonist. Anaptys is headquartered in San Diego, California, the US.

For a complete picture of Rosnilimab’s drug-specific PTSR and LoA scores, buy the report here.

This content was updated on 12 April 2024

Data Insights

From

The gold standard of business intelligence.

Blending expert knowledge with cutting-edge technology, GlobalData’s unrivalled proprietary data will enable you to decode what’s happening in your market. You can make better informed decisions and gain a future-proof advantage over your competitors.

GlobalData

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.