Trials / Recruiting
RecruitingNCT07099391
A Study of Dara-RVd and Teclistamab-RVd in People With Multiple Myeloma
ALTITUDE - ALTernating Induction Therapies to Achieve Undetectable Disease Endpoints: A Phase 1/2 Alternating Dara-RVd/Teclistamab-RVd in Transplant Eligible Standard-risk Newly Diagnosed Multiple Myeloma
- Status
- Recruiting
- Phase
- Phase 1 / Phase 2
- Study type
- Interventional
- Enrollment
- 65 (estimated)
- Sponsor
- Memorial Sloan Kettering Cancer Center · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to find out whether Tec-RVd (teclistamab, lenalidomide, bortezomib, and dexamethasone) after 3 treatment Cycles of Dara-RVd (daratumumab, lenalidomide, bortezomib, and dexamethasone) is a safe treatment for people with newly diagnosed multiple myeloma (MM).
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Dara-RVd | This study is a phase 1/2 study design of alternating 6 cycles of Dara-RVd/Tec-RVd induction therapy |
| DRUG | Tec-RVd | This study is a phase 1/2 study design of alternating 6 cycles of Dara-RVd/Tec-RVd induction therapy |
Timeline
- Start date
- 2025-07-24
- Primary completion
- 2029-07-24
- Completion
- 2029-07-24
- First posted
- 2025-08-01
- Last updated
- 2026-02-11
Locations
7 sites across 1 country: United States
Regulatory
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT07099391. Inclusion in this directory is not an endorsement.