COMPANY
Cogent Biosciences, Inc.
FDA-cleared device company Clinical Phase 3
Cogent Biosciences is a biotechnology company developing solutions to treat genetically driven diseases. From company website Source · Oct 12, 2026
Since the raise (Nov 11, 2025): 18 of 18 open jobs were first seen after it.
Hiring
| Title | Location (from posting) | Employer posted | First seen |
|---|---|---|---|
| Senior Manager, Medical Writing | Waltham, Massachusetts, United States | Oct 19, 2026 | Oct 20, 2026 |
| Senior Clinical Trial Associate | Waltham, Massachusetts, United States | Oct 14, 2026 | Oct 15, 2026 |
| Associate Director, Accounting Operations | Waltham, Massachusetts, United States | Oct 13, 2026 | Oct 14, 2026 |
| Associate Director, Training and Contract Operations | Waltham, Massachusetts, United States | Oct 8, 2026 | Oct 8, 2026 |
| Senior Associate, Pharmacovigilance Coordinator | Waltham, Massachusetts, United States | Oct 5, 2026 | Oct 8, 2026 |
Timeline
- Board tracked Radar started tracking this company’s job board (18 open jobs at last check). source ↗
- Trial start Phase 1: A Study of Mutant Selective-Inhibitor (CGT6297), in Patients With Advanced Solid Tumors source ↗
- Trial start Phase 1: A Study of a Selective ERBB2 Inhibitor (CGT4255), in Patients With Advanced Solid Tumors source ↗
- Debt Debt: $200M (not counted as a raise), announced Nov 12, 2025. Source: company release on GlobeNewswire. source ↗
- Raise Follow-on offering: $200M (total, as published), announced Nov 11, 2025. Source: SEC filing. source ↗
- Raise Follow-on offering: $230M (total, as published), announced Jul 10, 2025. Source: company release on GlobeNewswire. source ↗
- Debt Debt financing: $400M (up to, as announced), announced Jun 11, 2025. Source: company release on GlobeNewswire. source ↗
- Trial start Phase 1/Phase 2: A Study of an FGFR2/3 Inhibitor (CGT4859) in Patients With Cholangiocarcinoma and Other Advanced Solid Tumors source ↗
- Trial start Phase 2: (Summit) A Study to Evaluate the Efficacy and Safety of CGT9486 Versus Placebo in Patients With Indolent or Smoldering Systemic Mastocytosis source ↗
- Trial start 3: (Peak) A Phase 3 Randomized Trial of CGT9486+Sunitinib vs. Sunitinib in Subjects With Gastrointestinal Stromal Tumors source ↗
- Trial start Phase 2: (Apex) Bezuclastinib in Patients With Advanced Systemic Mastocytosis source ↗
- Trial start Phase 1: Study of ACTR T Cell Product in Combination With Trastuzumab in Subjects With HER2-Positive Advanced Solid Tumor Cancers source ↗
- Trial start Phase 1: Study of ACTR087 in Combination With SEA-BCMA in Subjects With Relapsed or Refractory Multiple Myeloma source ↗
- Trial start Phase 1: Study of ACTR707 in Combination With Rituximab in Subjects With Relapsed or Refractory B Cell Lymphoma source ↗
- Trial start —: Long-Term Follow-Up Study of Subjects Treated With ACTR T Cell Product source ↗
- Trial start Phase 1: Study of ACTR087 in Subjects With Relapsed or Refractory B-cell Lymphoma source ↗
- Trial start Phase 1/Phase 2: CGT9486 (Formerly Known as PLX9486) as a Single Agent and in Combination With PLX3397 (Pexidartinib) or Sunitinib in Participants With Advanced Solid Tumors source ↗
Upcoming milestones
- 2027-03 (ESTIMATED) · Phase 1/Phase 2 · A Study of an FGFR2/3 Inhibitor (CGT4859) in Patients With Cholangiocarcinoma and Other Advanced Solid Tumors · NCT06777316
- 2028-05 (ESTIMATED) · Phase 1 · A Study of a Selective ERBB2 Inhibitor (CGT4255), in Patients With Advanced Solid Tumors · NCT07361562
- 2029-07 (ESTIMATED) · Phase 1 · A Study of Mutant Selective-Inhibitor (CGT6297), in Patients With Advanced Solid Tumors · NCT07383506
Open jobs 18
| Title | Location (from posting, not HQ) | Employer posted | First seen | Level |
|---|---|---|---|---|
| Senior Manager, Medical Writing | Waltham, Massachusetts, United States | Oct 19, 2026 | Oct 20, 2026 | Not stated |
| Senior Clinical Trial Associate | Waltham, Massachusetts, United States | Oct 14, 2026 | Oct 15, 2026 | Senior |
| Associate Director, Accounting Operations | Waltham, Massachusetts, United States | Oct 13, 2026 | Oct 14, 2026 | Senior |
| Associate Director, Training and Contract Operations | Waltham, Massachusetts, United States | Oct 8, 2026 | Oct 8, 2026 | Senior |
| Senior Associate, Pharmacovigilance Coordinator | Waltham, Massachusetts, United States | Oct 5, 2026 | Oct 8, 2026 | Mid |
| Manager, Cost Accounting | Waltham, Massachusetts, United States | Oct 5, 2026 | Oct 8, 2026 | Mid |
| Senior Director, Global Market Access | Waltham, Massachusetts, United States | Sep 29, 2026 | Oct 8, 2026 | Senior |
| Scientist, DMPK (BioAnalytical and Medical Writing) | Boulder, Colorado, United States | Sep 28, 2026 | Oct 8, 2026 | Senior |
| Director, National Payer Accounts | Waltham, Massachusetts, United States | Sep 22, 2026 | Oct 8, 2026 | Senior |
| Director, Patient Advocacy & Engagement | Waltham, Massachusetts, United States | Sep 21, 2026 | Oct 8, 2026 | Senior |
| Manager, Communications and Investor Relations | Waltham, Massachusetts, United States | Sep 16, 2026 | Oct 8, 2026 | Mid |
| Associate Director, Translational Medicine | Waltham, Massachusetts, United States | Sep 14, 2026 | Oct 8, 2026 | Senior |
| Director, Corporate Counsel | Waltham, Massachusetts, United States | Sep 10, 2026 | Oct 8, 2026 | Senior |
| Contracts Specialist | Remote, United States | Aug 27, 2026 | Oct 20, 2026 | Not stated |
| Associate Director, Patient Marketing | Waltham, Massachusetts, United States | Jun 26, 2026 | Oct 8, 2026 | Senior |
| Principal Scientist, Computational Chemistry | Boulder, Colorado, United States | Apr 16, 2026 | Oct 8, 2026 | Senior |
| Senior Medical Science Liaison - West Region (Los Angeles, San Diego, Las Vegas, Mountain States {Idaho, Utah, Montana, Wyoming}) | Remote, United States | Mar 23, 2026 | Oct 8, 2026 | Senior |
| Research Investigator, Computational Chemistry | Boulder, Colorado, United States | Feb 18, 2026 | Oct 8, 2026 | Senior |
Funding
- Follow-on offering: $200M (total, as published), announced Nov 11, 2025. Source: SEC filing. source ↗
- Follow-on offering: $230M (total, as published), announced Jul 10, 2025. Source: company release on GlobeNewswire. source ↗
- Debt: $200M (not counted as a raise), announced Nov 12, 2025. Source: company release on GlobeNewswire. source ↗
- Debt financing: $400M (up to, as announced), announced Jun 11, 2025. Source: company release on GlobeNewswire. source ↗
Clinical trials (lead sponsor) 14
| Record | Title | Phase | Status | Start | Primary completion |
|---|---|---|---|---|---|
| NCT04996875 | (Apex) Bezuclastinib in Patients With Advanced Systemic Mastocytosis | Phase 2 | Recruiting | Nov 9, 2021 | Sep 19, 2025 (actual) |
| NCT07361562 | A Study of a Selective ERBB2 Inhibitor (CGT4255), in Patients With Advanced Solid Tumors | Phase 1 | Recruiting | Dec 30, 2025 | 2028-05 (estimated) |
| NCT07383506 | A Study of Mutant Selective-Inhibitor (CGT6297), in Patients With Advanced Solid Tumors | Phase 1 | Recruiting | Jul 23, 2026 | 2029-07 (estimated) |
| NCT06915766 | Expanded Access to Bezuclastinib for Patients With NonAdvanced Systemic Mastocytosis or Advanced Systemic Mastocytosis | Not listed | Available | Not listed | Not listed |
| NCT06948955 | Expanded Access to Bezuclastinib to be Coadministered With Sunitinib for Patients With Gastrointestinal Stromal Tumors | Not listed | Available | Not listed | Not listed |
| NCT05208047 | (Peak) A Phase 3 Randomized Trial of CGT9486+Sunitinib vs. Sunitinib in Subjects With Gastrointestinal Stromal Tumors | 3 | Recruiting | Apr 14, 2022 | Sep 30, 2025 (actual) |
| NCT05186753 | (Summit) A Study to Evaluate the Efficacy and Safety of CGT9486 Versus Placebo in Patients With Indolent or Smoldering Systemic Mastocytosis | Phase 2 | Active, not recruiting | Jun 27, 2022 | May 22, 2025 (actual) |
| NCT06777316 | A Study of an FGFR2/3 Inhibitor (CGT4859) in Patients With Cholangiocarcinoma and Other Advanced Solid Tumors | Phase 1/Phase 2 | Active, not recruiting | Jan 22, 2025 | 2027-03 (estimated) |
| NCT02401815 | CGT9486 (Formerly Known as PLX9486) as a Single Agent and in Combination With PLX3397 (Pexidartinib) or Sunitinib in Participants With Advanced Solid Tumors | Phase 1/Phase 2 | Completed | Mar 6, 2015 | May 11, 2020 (actual) |
| NCT03189836 | Study of ACTR707 in Combination With Rituximab in Subjects With Relapsed or Refractory B Cell Lymphoma | Phase 1 | Terminated | Oct 4, 2017 | Sep 21, 2020 (actual) |
| NCT02840110 | Long-Term Follow-Up Study of Subjects Treated With ACTR T Cell Product | Not listed | Terminated | 2016-10 | Oct 23, 2020 (actual) |
| NCT02776813 | Study of ACTR087 in Subjects With Relapsed or Refractory B-cell Lymphoma | Phase 1 | Completed | 2016-08 | Feb 12, 2020 (actual) |
| NCT03680560 | Study of ACTR T Cell Product in Combination With Trastuzumab in Subjects With HER2-Positive Advanced Solid Tumor Cancers | Phase 1 | Terminated | Mar 13, 2019 | Mar 12, 2020 (actual) |
| NCT03266692 | Study of ACTR087 in Combination With SEA-BCMA in Subjects With Relapsed or Refractory Multiple Myeloma | Phase 1 | Terminated | Feb 22, 2018 | Oct 1, 2019 (actual) |
Raises and investors new
- InvestorListed in the portfolio of Atlas Venture (captured Oct 12, 2026). portfolio page ↗
Connect
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