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Efficacy and Safety Study of Tisotumab Vedotin for Patients With Solid Tumors

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NCT03485209

Sponsored by Seagen, a wholly owned subsidiary of Pfizer (industry) · PFE — their whole pipeline →. With Genmab, Merck Sharp & Dohme LLC.

Phase
Phase 2
Status
Active, not recruiting
Study type
Interventional
Design
Non randomized · None · Treatment
Enrollment
350actual
Sites
175
Countries
Canada, France, Germany +4

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2018-06-25actualWhen the study began enrolling
Primary completion2026-03-20actualThe date the last participant is measured for the primary outcome — the readout window
Study completion2027-03-31estimatedThe whole study's end, after follow-up
First posted2018-04-02actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-07-22actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • Colorectal Neoplasms
  • Carcinoma, Non-Small-Cell Lung
  • Exocrine Pancreatic Cancer
  • Carcinoma, Squamous Cell of Head and Neck

Interventions

  • Drug: tisotumab vedotin — also filed as TIVDAK
  • Drug: pembrolizumab — also filed as KEYTRUDA®
  • Drug: carboplatin
  • Drug: cisplatin

Primary outcome

what the primary-completion date above is the date OF
Confirmed Objective Response Rate (ORR) (Parts A, B, C, D, E, F, and G)
measured Up to approximately 3 years

Publications

Linked on the registry record. A “linked by the registry” entry is NLM's own automated PubMed match, not a claim by the sponsor that the paper reports this study.

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