A Phase 1, Open-Label, Dose-Escalation Study to Evaluate Safety, Tolerability, and Clinical Activity of CBX-663 in Participants With Relapsed or Refractory Myeloid Malignancies, Advanced Solid Tumors, or Recurrent or Progressive Glioblastoma.
Part of paid clinical trials in Fairfax, Virginia.
- Sponsor
- Crossbow Therapeutics, Inc.
- Study ID
- NCT07779798
- Phase
- PHASE1
- Status
- Not Yet Recruiting
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Conditions
- Advanced Solid Tumors
- Recurrent or Progressive Glioblastoma
- Relapse or Refractory Myeloid Malignancies
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- CBX-663 — DRUGIntravenous (I.V.) CBX-663
Study Details
This is a Phase 1, open-label, dose-escalation study of CBX-663 in participants with R/R AML, MDS or CMML (Cohort A), advanced solid tumors (Cohort B), or recurrent or progressive GBM (Cohort C) (collectively called 'indication cohorts'). Participants aged ≥18 years are planned to be enrolled. CBX-663 will initially be investigated on a fixed dosing schedule. CBX-663 will be administered intravenously (IV) on Cycle 1 Day 1 (C1D1) and then once weekly (QW) in 21-day cycles. Participants will continue treatment with CBX-663 until unacceptable toxicity, progressive disease, withdrawal of consent, or lack of clinical benefit.
Key Dates
- First listed
- Aug 21, 2026
- Start date
- Aug 31, 2026
- Status verified
- Aug 2026
- Primary completion
- Jan 31, 2028
- Completion
- Jun 30, 2028
Study Design
- Enrollment
- 120 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: CBX-663Intravenous (I.V.) CBX-663
Primary Outcome Measure
Recommended Phase 2 Dose (RP2D) [ Time Frame: Until the end of study (approximately 24 months) ]
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| NEXT Oncology- Virginia | Fairfax | Virginia | 22031 | Alexander Spira, MD (PRINCIPAL_INVESTIGATOR) |
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