MK4280A-010
Fase 2 MK-4280A -co-formulatie van Favezelimab (MK-4280) en Pembrolizumab (MK-3475) – bij geselecteerde solide tumoren (Cohort A:cSCC / Cohort B: pMMR EC) A randomized, double-blind, placebo-controlled phase 2,…
Fase 2 MK-4280A -co-formulatie van Favezelimab (MK-4280) en Pembrolizumab (MK-3475) – bij geselecteerde solide tumoren (Cohort A:cSCC / Cohort B: pMMR EC) A randomized, double-blind, placebo-controlled phase 2,…
Studiecoördinator Dr. S.F. Oosting Afdeling Medische Oncologie Tel.: 050 3612821 (secretariaat Oncologie) E-mail: s.f.oosting@umcg.nl
(Peak) A Phase 3 Randomized, Open-label, Multicenter Clinical Study of CGT9486+Sunitinib vs Sunitinib in Subjects with Locally Advanced, Unresectable, or Metastatic Gastrointestinal Stromal Tumors Samenvatting Dit is een…
ANZadapt studie Phase II randomised controlled trial of patient-specific adaptive versus continuous Abiraterone or eNZalutamide in metastatic castration-resistant prostate cancer: the ANZadapt study Samenvatting De ANZadapt studie is…
A Randomized, Open-label, Phase 3 Study of Sacituzumab Govitecan and Pembrolizumab Versus Treatment of Physician’s Choice and Pembrolizumab in Patients With Previously Untreated, Locally Advanced Inoperable or Metastatic…
A Randomized, Open-label, Phase 3 Study of Sacituzumab Govitecan Versus Treatment of Physician’s Choice in Patients With Previously Untreated, Locally Advanced, Inoperable or Metastatic Triple-Negative Breast Cancer Whose…
A Multi-center, Double-Blind, Randomized Phase 3 Study to Compare the Efficacy and Safety of Belzutifan (MK-6482) plus Pembrolizumab (MK- 3475) Versus Placebo plus Pembrolizumab, in the Adjuvant Treatment…
A Phase I Study to Assess Biodistribution of 89Zr-CB307 in PSMA+ and PSMA-Tumour Lesions Eudractnummer: 2021-006256-13 CB307 is een trispecifieke Humabody® gericht op CD137; PSMA; en humaan serumalbumine…
A Phase 3, Randomized, Double-Blind, Placebo-Controlled Study of Abemaciclib in Combination with Abiraterone plus Prednisone in Men with High-Risk Metastatic Hormone-Sensitive Prostate Cancer EU trial number: 2022-500461-28-06 Samenvatting…
A 3 arm randomized study on health-related quality of life of elderly patients with advanced soft tissue sarcoma undergoing doxorubicin every three weeks or doxorubicin weekly or cyclophosphamide…
A Phase 1a/1b Study exploring the safety and tolerability of INCB081776 +/- retifanlimab in participants with advanced malignancies Protocol: INCB 81776-101 EudraCT Number: 2020-004867-26 Een Fase 1a/1b, open label…
A Phase 1a/1b Study exploring the safety and tolerability of INCB081776 +/- retifanlimab in participants with advanced malignancies Protocol: INCB 81776-101 EudraCT Number: 2020-004867-26 Een Fase 1a/1b, open label…
A Phase 3 Randomized, Open-label, Active-comparator Controlled Clinical Study of Pembrolizumab versus Platinum Doublet Chemotherapy in Participants With Mismatch Repair Deficient (dMMR) Advanced or Recurrent Endometrial Carcinoma in…
Behandeling met cemiplimab van patiënten met lokaal vergevorderd of gemetastaseerd secundair angiosarcoom. Eudractnummer: 2020-005465-13 Samenvatting In deze fase II studie kunnen patiënten met een lokaal vergevorderd of gemetastaseerd…
Een nationaal, multicenter, niet-geblindeerde doelmatigheids studie waarbij zes maanden avelumab onderhoudsbehandeling wordt gegeven aan patienten met een lokaal gevorderd of gemetastaseerde urotheelcarcinoom zonder ziekteprogressie na minimaal 4 kuren…
Phase III Randomized, Open-Label, Multicenter Study to Determine the Efficacy and Safety of Durvalumab in Combination With Tremelimumab and Enfortumab Vedotin or Durvalumab in Combination With Enfortumab Vedotin…
Randomized, double-blind, phase 3 study of tucatinib or placebo in combination with ado-trastuzumab emtansine (T-DM1) for subjects with unresectable locally-advanced or metastatic HER2+ breast cancer Protocolnummer: SGNTUC-016 Eudractnummer:…
A Phase 1 Open-Label, Dose Escalation and Expansion Trial to Investigate the Safety, harmacokinetics and Pharmacodynamics of CB307, a Trispecific Humabody® T-cell Enhancer, in Patients with PSMA+ Advanced…