First In Human Study of CX-801 in Advanced Solid Tumors
Part of paid clinical trials in Englewood, Colorado.
- Sponsor
- CytomX Therapeutics
- Study ID
- NCT06462794
- Phase
- PHASE1
- Status
- Recruiting
Conditions
- Solid Tumor, Adult
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- CX-801 — DRUGInvestigational drug
- pembrolizumab — DRUGStandard of Care Therapy
Study Details
The purpose of this first-in-human study, CTMX-801-101, is to characterize the safety, tolerability, and antitumor activity of CX-801 as monotherapy and in combination with pembrolizumab in adult participants with advanced solid tumors.
Key Dates
- Start date
- Aug 28, 2024
- Status verified
- May 2026
- Primary completion
- Feb 28, 2028
- Completion
- Jun 30, 2029
Study Design
- Enrollment
- 121 participants (estimated)
- Allocation
- NON_RANDOMIZED
- Intervention model
- SEQUENTIAL
- Primary purpose
- TREATMENT
Arms
- Experimental: CX-801
- Experimental: CX-801 + pembrolizumab
Primary Outcome Measure
Safety and tolerability of CX-801 as monotherapy and combination therapy [ Time Frame: 44 months ]
Central Contacts
- Karen Deane650-515-3185
Locations (3)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| The Melanoma and Skin Cancer Institute | Englewood | Colorado | 80113 | - |
| University of Pittsburgh Hillman Cancer Center | Pittsburgh | Pennsylvania | 15232 | - |
| SCRI Oncology Partners | Nashville | Tennessee | 37203 | - |
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