PER-001 is under clinical development by Perfuse Therapeutics and currently in Phase II for Diabetic Retinopathy. According to GlobalData, Phase II drugs for Diabetic Retinopathy have a 53% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how PER-001’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.

PER-001 overview

PER-001 is under development for the treatment of open-angle glaucoma, diabetic retinopathy geographic atrophy and retinal vein occlusion. The drug candidate is a small molecular endothelin 1 receptor antagonist and is administered as intravitreal implant.

Perfuse Therapeutics overview

Perfuse Therapeutics, a clinical-stage biopharmaceutical company developing therapies for the treatment of eye disease, retinal perfusion. The company is headquartered in San Francisco, California, the US.

For a complete picture of PER-001’s drug-specific PTSR and LoA scores, buy the report here.

This content was updated on 10 June 2024

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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.