10 mg/ml
Sponsors
Bristol-Myers Squibb International Corporation, Immunogen Inc., Dbv Technologies, Bristol-Myers Squibb Services Unlimited Company, Narodowy Instytut Onkologii Im. Marii Sklodowskiej-Curie-Panstwowy Instytut Badawczy
Conditions
Advanced throat and larynx cancerEarly Stage Non-Small Cell Lung Cancer (NSCLC)HER2 negative breast cancerHealthy volunteersLung CancerMale and female participants ≥ 18 years of age with advanced or
metastatic cancersNon-urgent non-cardiac surgical procedure or relative emergency >12h that will require curarisation with rocuronium and decurarisation with sugammadexPeanut allergy
Phase 1
A Phase 1/2 Study of BMS-986340 as Monotherapy and in Combination with Nivolumab or
Docetaxel in Participants with Advanced Solid Tumors
RecruitingCTIS2023-503651-10-00
Start: 2022-05-17Target: 163Updated: 2025-12-04
Study of RMC-6291, With or Without RMC-6236, in Combination With Other Anti-Cancer Agents, in Patients With RAS G12C-Mutated Non-Small Cell Lung Cancer – Subprotocol A
RecruitingCTIS2023-509571-16-00
Start: 2024-07-17Target: 162Updated: 2025-12-17
A Phase 1b/2 Open-Label, Multicenter Study of RMC-6236 in Combination with Pembrolizumab with or without Chemotherapy, in Patients with RAS‑Mutated Non-Small Cell Lung Cancer (NSCLC) – Subprotocol B
RecruitingCTIS2023-509572-42-00
Start: 2024-07-17Target: 180Updated: 2026-01-13
Phase 2
A phase II study of preoperative stereotactic radiation therapy boost combined with short-course immunotherapy (pembrolizumab versus placebo, randomized, double-blind) and standard chemotherapy in patients with newly diagnosed HER2-negative non-metastatic breast cancer with lack of early metabolic response in 18-fluorodeoxyglucoseFDG-PET/CT after 1st chemoterapy cycle
RecruitingCTIS2023-504145-31-00
Start: 2024-06-10Target: 78Updated: 2024-02-21
Morphine effects on stress response and social interaction – an exploratory randomized controlled experimental medicine study
Active, not recruitingCTIS2024-517855-10-00
Start: 2022-04-20Target: 36Updated: 2024-10-25
The asssessment of the efficacy of induction radiochemotherapy using low doses of ionizing radiation (iCHRTL) in the treatment of patients with advanced throat and larynx cancer
RecruitingCTIS2024-517480-23-00
Start: 2022-02-17Target: 40Updated: 2025-01-31
A DOSE-DETERMINATION STUDY OF SUGAMMADEX AS A ROCURONIUM DECURARIZATION AGENT IN CHILDREN UNDER 2 YEARS OF AGE
Not yet recruitingCTIS2025-521946-82-00
Target: 99Updated: 2025-11-12
Phase 3
Randomized, Open-Label, Phase 3 Trial of Nivolumab plus Ipilimumab or Nivolumab plus Platinum-Doublet Chemotherapy versus Platinum-Doublet
Chemotherapy in Early Stage NSCLC
CompletedCTIS2022-501360-18-00
Start: 2017-03-15End: 2024-12-03Target: 194Updated: 2024-12-03
A Phase 3, Double-blind, Placebo-controlled, Randomized Study to Assess the Efficacy and Safety of Epicutaneous Immunotherapy with DBV712 250 μg in 4-7-year-old Children with Peanut Allergy (VITESSE)
Active, not recruitingCTIS2022-502110-85-00
Start: 2024-01-18Target: 126Updated: 2025-12-15
A Phase 3, Randomized, Double-blind Study of Neoadjuvant Chemotherapy plus Nivolumab versus Neoadjuvant Chemotherapy plus Placebo, followed by Surgical Resection and Adjuvant Treatment with Nivolumab or Placebo for Participants with Resectable Stage II-IIIB Non-small Cell Lung Cancer (CheckMate 77T, CHECKpoint pathway and nivoluMAb clinical Trial Evaluation 77T)
Active, not recruitingCTIS2022-502658-15-00
Start: 2019-09-22Target: 252Updated: 2025-10-08
2022-501606-35-00 – Randomized, multicenter, open-label, Phase 3 study of mirvetuximab soravtansine in combination with bevacizumab versus bevacizumab alone as maintenance therapy for patients with FRα-high recurrent platinum-sensitive epithelial ovarian, fallopian tube, or primary peritoneal cancers who have not progressed after second-line platinum-based chemotherapy plus bevacizumab (GLORIOSA).
RecruitingCTIS2022-501606-35-01
Start: 2024-02-21Target: 110Updated: 2026-01-21
A Phase 3, Double-Blind, Placebo-Controlled, Randomized Study to Assess the Safety of Epicutaneous Immunotherapy with DBV712 250 µg in 1-through 3-year-old Children with Peanut Allergy
RecruitingCTIS2025-521697-34-00
Start: 2025-12-01Target: 54Updated: 2026-01-21