BioXcel Therapeutics
BTAIBTAI · Stock Price
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Overview
BioXcel Therapeutics' mission is to accelerate and de-risk drug development by applying artificial intelligence to identify new therapeutic applications for existing pharmacologically active compounds. Its primary achievement is the 2022 FDA approval and ongoing commercialization of IGALMI® for acute agitation, with a pivotal near-term catalyst being the FDA's review of a supplemental New Drug Application (sNDA) for at-home use. The company's strategy centers on expanding the label and market reach of its lead asset while advancing its pipeline, including BXCL501 for opioid withdrawal and agitation in Alzheimer's disease, and BXCL701 in immuno-oncology, though its financial position is constrained, necessitating recent capital raises.
Technology Platform
Proprietary AI and machine learning platform that mines biomedical data to identify novel therapeutic applications for existing pharmacologically active compounds, accelerating and de-risking drug development.
Pipeline
18| Drug | Indication | Stage | Watch |
|---|---|---|---|
| Sublingual film containing Igalmi | Bipolar Disorder | Approved | |
| Dexmedetomidine + Lorazepam 2 MG/ML | Schizophrenia Agitation | Approved | |
| Sublingual film containing Dexmedetomidine (BXCL501) + Place... | Agitation Associated With Bipolar Disorder | Phase 3 | |
| BXCL501 + Matching Placebo | Agitation | Phase 3 | |
| BXCL501 + Matching Placebo | Agitation,Psychomotor | Phase 3 |
Funding History
3Opportunities
Risk Factors
Competitive Landscape
Faces competition from generic injectable/oral antipsychotics and benzodiazepines in acute agitation, and from newly approved brexpiprazole in Alzheimer's agitation. In opioid withdrawal, competes with clonidine, lofexidine, and opioid therapies.