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Taking peoplePhase 2

Tests SKB264 with pembrolizumab in several solid tumor types

Tests SKB264 with pembrolizumab in adults with selected solid tumors.

Plain-language title generated from the registry record
Registry title: A basket study to investigate the efficacy and safety of SKB264 in combination with pembrolizumab in subjects with solid tumors

Key facts

Where
Brasschaat, Charleroi, and Sint-Lambrechts-Woluwe, BelgiumSee the 3 sites
Phase
Phase 2

Where in Belgium

  • AZ KLINABrasschaat, BelgiumNo longer taking part
  • Grand Hopital de CharleroiCharleroi, BelgiumNo longer taking part
  • Cliniques Universitaires Saint-LucSint-Lambrechts-Woluwe, BelgiumNo longer taking part

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
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Trial details

Who runs it
Sichuan Kelun-Biotech Biopharmaceutical Co. Ltd.
Trial code
NCT05642780EU 2022-502654-14-00
Record updated
19 May 2026
Original description
The main purpose of this study is to see if SKB264 in combination with pembrolizumab is safe and effective in treating selected solid tumors.Read full original descriptionShow less

A multicenter, open-label, phase 2, basket study to evaluate the efficacy and safety of SKB264 in combination with pembrolizumab in subjects with selected solid tumors

The main purpose of this study is to see if SKB264 in combination with pembrolizumab is safe and effective in treating selected solid tumors.

Inclusion: Male and/or females of age 18 years and older who have histologically or cytologically confirmed locally advanced or metastatic cancer or recurrent cancer (Cervical, Urothelial, Ovarian, Prostate or Endometrial cancer).

Exclusion: Subjects who received any chemotherapy, radiotherapy, immunotherapy, or biologic therapy treatment within 4 weeks before the first dose of the study drug; Subjects with hepatitis B, hepatitis C, human immunodeficiency virus (HIV) or active Tuberculosis; Subjects with a history of allogeneic tissue or solid organ transplant; Subjects with active central nervous system tumors or metastases.

ClinicalTrials.gov NCT05642780 · EU CTIS 2022-502654-14-00