drugset / Trial / NCT03033914
A(B)VD Followed by Nivolumab as Frontline Therapy for Higher Risk Patients With Classical Hodgkin Lymphoma (HL)
Phase 1/2
Active not recruiting
82 enrolled
Memorial Sloan Kettering Cancer Center
Barbara Ann Karmanos Cancer Institute · collabBristol-Myers Squibb · collabBritish Columbia Cancer Agency · collab
Non-randomizedParallel-groupOpen-labelTreatment
Summary
The aim of this study is to improve the chance of cure for people with higher risk Hodgkin lymphoma. The purpose of the Phase I study is to test any good and bad effects of the study drug called Nivolumab when combined with ABVD for the front-line treatment of HL.The purpose of this Phase II study is to test whether including nivolumab in treatment for untreated Hodgkin lymphoma can improve the chance of cure for patients with abnormal PET scans after 2 cycles of ABVD.
Timeline
- Start
- 2017-01-25
- Primary completion
- 2027-01
- Completion
- 2027-01
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Nivolumab | Monoclonal antibody | 240 mg | Intravenous |
| Background | Bleomycin | Unknown | 10 unknown | Intravenous |
| Background | Dacarbazine | Small molecule | 375 mg/m2 | Intravenous |
| Background | Doxorubicin | Other / unclassified | 25 mg/m2 | Intravenous |
| Background | Vinblastine | Small molecule | 6 mg/m2 | Intravenous |