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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.

Phase 1RecruitingSeagen, a wholly owned subsidiary of PfizerNCT04389632Data as of May 2026

Treatment: sigvotatug vedotin · pembrolizumab · cisplatin · carboplatinThis 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.

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Extracted 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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