COMPANY
BioXcel Therapeutics
FDA-approved therapeutic company Clinical Phase 3
Timeline
- FDA FDA New indication / efficacy supplement: IGALMI (dexmedetomidine hydrochloride) — NDA215390/2, Nov 19, 2025. Applicant at approval: BioXcel Therapeutics, Inc. source ↗
- Trial start Phase 2: Assessment of Acute Psychomotor Agitation Measures Associated With Schizophrenia and Bipolar Disorder source ↗
- Raise Follow-on offering — Registered direct: $14M (total, as published), announced Mar 3, 2025. Source: company release on GlobeNewswire. source ↗
- Grant Government grant: $2.8M (total, as published), announced Oct 15, 2024. Source: company release on GlobeNewswire. source ↗
- Trial start Phase 4: Tachyphylaxis, Tolerance, & Withdrawal Post Treatment With Igalmi for Agitation in Schizophrenia or Bipolar Disorder source ↗
- Trial start Phase 3: Dexmedetomidine in the Treatment of Agitation Associated With Dementia (TRANQUILITY III) source ↗
- Trial start Phase 3: Dexmedetomidine in the Treatment of Agitation Associated With Schizophrenia and Bipolar Disorder (SERENITY III) source ↗
- Trial start Phase 3: Dexmedetomidine in the Treatment of Agitation Associated With Dementia (TRANQUILITY II) source ↗
- Trial start Phase 2: An Efficacy, and Safety Study Of BXCL501 For The Treatment Of Agitation Associated With Dementia source ↗
- Trial start Phase 1: Determining Efficacy and Safety of BXCL501 in Agitation Associated With Pediatric Schizophrenia and Bipolar Disorder source ↗
- Trial start Phase 2: Study of BXCL501 In Agitation Associated With Delirium in ICU Patients source ↗
- Trial start Phase 1/Phase 2: Dexmedetomidine in the Treatment of Symptoms Of Acute Opioid Withdrawal source ↗
- Trial start Phase 3: Dexmedetomidine in the Treatment of Agitation Associated With Bipolar Disorder source ↗
- Trial start Phase 3: Dexmedetomidine in the Treatment of Agitation Associated With Schizophrenia source ↗
- Trial start Phase 1/Phase 2: Sub-Lingual Dexmedetomidine in Agitation Associated With Dementia source ↗
- Trial start Early phase 1: A Pilot Study of BXCL701 in Patients With Pancreatic Cancer source ↗
- Trial start Phase 1: Sub-Lingual Dexmedetomidine in Agitation Associated With Schizophrenia source ↗
- Trial start Phase 1/Phase 2: A Trial of BXCL701 and Pembrolizumab in Patients With mCRPC Either Small Cell Neuroendocrine Prostate Cancer or Adenocarcinoma Phenotype. source ↗
Upcoming milestones
- Jul 31, 2027 (ESTIMATED) · Phase 1 · Determining Efficacy and Safety of BXCL501 in Agitation Associated With Pediatric Schizophrenia and Bipolar Disorder · NCT05025605
Funding
Clinical trials (lead sponsor) 15
| Record | Title | Phase | Status | Start | Primary completion |
|---|---|---|---|---|---|
| NCT07116694 | Assessment of Acute Psychomotor Agitation Measures Associated With Schizophrenia and Bipolar Disorder | Phase 2 | Completed | Jun 19, 2025 | Oct 7, 2025 (actual) |
| NCT05665088 | Dexmedetomidine in the Treatment of Agitation Associated With Dementia (TRANQUILITY III) | Phase 3 | Terminated | Dec 5, 2022 | Sep 11, 2023 (actual) |
| NCT05271552 | Dexmedetomidine in the Treatment of Agitation Associated With Dementia (TRANQUILITY II) | Phase 3 | Completed | Apr 27, 2022 | Apr 21, 2023 (actual) |
| NCT05025605 | Determining Efficacy and Safety of BXCL501 in Agitation Associated With Pediatric Schizophrenia and Bipolar Disorder | Phase 1 | Recruiting | Aug 27, 2021 | Jul 31, 2027 (estimated) |
| NCT05276830 | An Efficacy, and Safety Study Of BXCL501 For The Treatment Of Agitation Associated With Dementia | Phase 2 | Terminated | Feb 8, 2022 | Apr 1, 2022 (actual) |
| NCT04123574 | A Pilot Study of BXCL701 in Patients With Pancreatic Cancer | Early phase 1 | Withdrawn | Oct 15, 2019 | Dec 6, 2021 (estimated) |
| NCT06041646 | Tachyphylaxis, Tolerance, & Withdrawal Post Treatment With Igalmi for Agitation in Schizophrenia or Bipolar Disorder | Phase 4 | Completed | Oct 2, 2023 | Apr 29, 2024 (actual) |
| NCT04276883 | Dexmedetomidine in the Treatment of Agitation Associated With Bipolar Disorder | Phase 3 | Completed | Feb 24, 2020 | May 21, 2020 (actual) |
| NCT04251910 | Sub-Lingual Dexmedetomidine in Agitation Associated With Dementia | Phase 1/Phase 2 | Completed | Dec 27, 2019 | Jan 24, 2022 (actual) |
| NCT04268303 | Dexmedetomidine in the Treatment of Agitation Associated With Schizophrenia | Phase 3 | Completed | Jan 24, 2020 | May 6, 2020 (actual) |
| NCT04470050 | Dexmedetomidine in the Treatment of Symptoms Of Acute Opioid Withdrawal | Phase 1/Phase 2 | Completed | Jun 9, 2020 | Feb 18, 2021 (actual) |
| NCT04010305 | Sub-Lingual Dexmedetomidine in Agitation Associated With Schizophrenia | Phase 1 | Completed | May 22, 2019 | Jul 31, 2019 (actual) |
| NCT05313386 | Study of BXCL501 In Agitation Associated With Delirium in ICU Patients | Phase 2 | Withdrawn | Feb 23, 2021 | Feb 21, 2022 (estimated) |
| NCT05658510 | Dexmedetomidine in the Treatment of Agitation Associated With Schizophrenia and Bipolar Disorder (SERENITY III) | Phase 3 | Completed | Nov 21, 2022 | Aug 15, 2025 (actual) |
| NCT03910660 | A Trial of BXCL701 and Pembrolizumab in Patients With mCRPC Either Small Cell Neuroendocrine Prostate Cancer or Adenocarcinoma Phenotype. | Phase 1/Phase 2 | Completed | Feb 12, 2019 | Oct 31, 2023 (actual) |
FDA records (last 2 years)
- FDA New indication / efficacy supplement: IGALMI (dexmedetomidine hydrochloride) — NDA215390/2, Nov 19, 2025. Applicant at approval: BioXcel Therapeutics, Inc. source ↗
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