A Study of XmAb®23104 in Subjects With Selected Advanced Solid Tumors (DUET-3)
Part of paid clinical trials in San Diego, California.
- Sponsor
- Xencor, Inc.
- Study ID
- NCT03752398
- Phase
- PHASE1
- Status
- Completed
Conditions
- Advanced Solid Tumors
- Breast Carcinoma That is Estrogen Receptor, Progesterone Receptor, and Her2 Negative
- Cervical Carcinoma
- Colorectal Carcinoma
- Endometrial Carcinoma
- Gastric or Gastroesophageal Junction Adenocarcinoma
- Hepatocellular Carcinoma
- Melanoma (Excluding Uveal Melanoma)
- Nasopharyngeal Carcinoma
- Non-small Cell Lung Carcinoma
- Pancreatic Carcinoma
- Renal Cell Carcinoma
- Small Cell Lung Cancer
- Squamous Cell Carcinoma of the Head and Neck
- Undifferentiated Pleomorphic Sarcoma
- Urothelial Carcinoma
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- XmAb®23104 — BIOLOGICALMonoclonal bispecific antibody
- Yervoy® (ipilimumab) — BIOLOGICALMonoclonal antibody
Study Details
This is a Phase 1, multiple dose, ascending dose escalation study to define a MTD/RD and regimen of XmAb23104, to describe safety and tolerability, to assess PK and immunogenicity, and to preliminarily assess anti-tumor activity of XmAb23104 monotherapy and combination therapy with ipilimumab in subjects with selected advanced solid tumors.
Key Dates
- Start date
- May 1, 2019
- Status verified
- Jul 2024
- Primary completion
- Feb 15, 2024
- Completion
- Feb 15, 2024
Study Design
- Enrollment
- 198 participants (actual)
- Allocation
- RANDOMIZED
- Intervention model
- SEQUENTIAL
- Primary purpose
- TREATMENT
Arms
- Experimental: XmAb®23104 MonotherapyXmAb®23104 administered by IV dosing on Days 1 and 15 of each 28-day cycle x 2 cycles
- Experimental: XmAb®23104 Combination Therapy with IpilimumabXmAb®23104 administered by IV on Days 1 and 15 of each 28-day cycle x 2 cycles + Yervoy® (ipilimumab)
Primary Outcome Measure
Treatment-related adverse events as assessed by CTCAE v4.03 [ Time Frame: 56 Days ]
Locations (18)
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