BMND-07 is under clinical development by Biomind Labs and currently in Phase I for Major Depressive Disorder. According to GlobalData, Phase I drugs for Major Depressive Disorder have an 85% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how BMND-07’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.

BMND-07 overview

BMND-07 is under development for the treatment of major depressive disorder. It is a DMT combination drug which acts by targeting 5-hydroxytryptamine receptor 1A, 2A and 2C (5HT1A, 5HT2A and 5HT2C).

Biomind Labs overview

Biomind Labs, formely Crosswinds is an equity firm and asset manager that invests in the financial services sector. The company operates its business through a value chain including insurance, reinsurance and asset management sectors, among others. Its Monarch National Insurance Company, provides Monarch platform, which is a property and casualty insurance carrier operating in the US. Crosswind offers major subsidiaries such as Crosswinds AUM LLC, Crosswinds Monarch GP LLC, Crosswinds Re, Crosswinds Private Equity Partners (C.I.), GP, Crosswinds Private Equity Partners (C.I.), LP, and Crosswinds Investor Monarch LP, among others. The company operates in Canada and the US. Biomind Labs is headquartered in Toronto, Canada.

For a complete picture of BMND-07’s drug-specific PTSR and LoA scores, buy the report here.

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 its clinical pathway (PTSR), as well as how likely the drug will be approved (LoA). This is based on a proprietary algorithm built from the drugs’ sales forecast, regulatory milestones, cost forecasts, WACC rate and other proprietary data sources found on GlobalData’s Pharmaceutical Intelligence Center.