OncoMatch/Clinical Trials/NCT04389632
A Study of Sigvotatug Vedotin in Advanced Solid Tumors
Is NCT04389632 recruiting? Yes, currently enrolling (May 2026). This Phase 1 trial studies multiple treatments including sigvotatug vedotin and pembrolizumab for carcinoma, non-small cell lung.
Treatment: sigvotatug vedotin · pembrolizumab · cisplatin · carboplatin — This trial will look at a drug called sigvotatug vedotin (SGN-B6A) alone and with pembrolizumab, with or without chemotherapy, to find out whether it is safe for people who have solid tumors. It will study sigvotatug vedotin to find out what its side effects are. A side effect is anything the drug does besides treating cancer. It will also study whether sigvotatug vedotin works to treat solid tumors. The study will have four parts. * Part A of the study will find out how much sigvotatug vedotin should be given to participants. * Part B will use the dose found in Part A to find out how safe sigvotatug vedotin is and if it works to treat solid tumors. * Part C of the study will find out how safe sigvotatug vedotin is in combination with these other drugs. * Part D will include people who have not received treatment. This part of the study will find out how safe sigvotatug vedotin is in combination with these other drugs and if these combinations work to treat solid tumors. * In Parts C and D, participants will receive sigvotatug vedotin with either: * Pembrolizumab or, * Pembrolizumab and carboplatin, or * Pembrolizumab and cisplatin.
Check if I qualifyExtracted eligibility criteria
Cancer type
Non-Small Cell Lung Carcinoma
Head and Neck Squamous Cell Carcinoma
Breast Carcinoma
Esophageal Carcinoma
Gastric Cancer
Ovarian Cancer
Pancreatic Cancer
Urothelial Carcinoma
Cervical Cancer
Disease stage
Metastatic disease required
Performance status
ECOG 0–1(Restricted strenuous activity)
Prior therapy
Must have received: platinum-based chemotherapy
Part B only: Participants must have received platinum-based therapy
Must have received: anti-PD-1/PD-L1 therapy
Part B only: Participants must have received ... a PD-1/PD-(L)1 inhibitor, if applicable and available
Cannot have received: MMAE-containing agent
Previous receipt of an MMAE-containing agent
Cannot have received: agent targeting integrin beta-6
Previous receipt of ... an agent targeting integrin beta-6
Structured fields extracted by AI. May contain errors — verify against the official protocol.
US trial sites
- Alaska Oncology and Hematology · Anchorage, Alaska
- Highlands Oncology Group · Fayetteville, Arkansas
- Highlands Oncology Group · Rogers, Arkansas
- Highlands Oncology Group · Springdale, Arkansas
- Providence Medical Foundation · Anaheim, California
Showing up to 5 US sites. See all sites on ClinicalTrials.gov →
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