Debio-4126 is under clinical development by Debiopharm International and currently in Phase I for Neuroendocrine Gastroenteropancreatic Tumors (GEP-NET). According to GlobalData, Phase I drugs for Neuroendocrine Gastroenteropancreatic Tumors (GEP-NET) have a 97% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how Debio-4126’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.

Debio-4126 overview

Debio-4126 is under development for the treatment of gastroenteropancreatic neuroendocrine tumors and acromegaly. It is a sustained release formulation. It is administered through intramuscular route and It is being developed based on modified-release Debiosphere technology The therapeutic candidate is an analogue of somatostatin.

Debiopharm International overview

Debiopharm International, a subsidiary of Debiopharm Group, focuses on the development and manufacture of drugs for oncology and bacterial infections. The company offers oxaliplatin and triptorelin drugs. It is investigating proteins, peptides and small molecules to treat cancers, solid tumors, bone and joint infections and gastrointestinal disorders. Debiopharm is headquartered in Lausanne, Switzerland.

For a complete picture of Debio-4126’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.