INVA-8002 is under clinical development by Invea Therapeutics and currently in Phase I for Irritable Bowel Syndrome. According to GlobalData, Phase I drugs for Irritable Bowel Syndrome have an 82% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how INVA-8002’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.

INVA-8002 overview

INVA-8002 is under development for the treatment of ulcerative colitis in combination with anti-TNF regimen and irritable bowel syndrome (IBS). It is a new chemical entity. It is being developed based on artificial intelligence AI-powered AlphaMeld technology platform.

Invea Therapeutics overview

Invea Therapeutics (Invea) is a biotechnology company focuses on the discovery of therapeutics for gastrointestinal and hepatobiliary disorders. Invea is headquartered in Guilford, Connecticut,the US.

For a complete picture of INVA-8002’s drug-specific PTSR and LoA scores, buy the report here.

This content was updated on 2 September 2023

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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.