Live from ClinicalTrials.gov + Open Targets, fetched 2026-11-11 16:07 UTC. Every row links to its source record.
Postmortem · what the sponsor and named sources said, kept apart from what merely happened at the same time
A Study of Daratumumab With Pomalidomide, Dexamethasone, and All-Transretinoic Acid in Patients With Multiple Myeloma
NCT04700176 · Hackensack Meridian Health · PHASE2 · terminated · last registry update 2025-02-25 · Multiple myeloma · Decision brief
No research has been run for this trial yet, so only the registry's own reason and the timeline are shown.
What was said, and by whom
Stated is the sponsor's own words; Reported is a named third party. The category is our label from a fixed list; the quote is the evidence.
| Kind | Quote | Our category | Source |
|---|---|---|---|
| Stated | “Low Accrual” | Open Targets' class: insufficient enrollment | Registry record, Hackensack Meridian Health |
Also happening at the time. Not shown to be a cause.
Registry events on other trials of drugs against CD38 in multiple myeloma within 12 months either side of this trial's last update, live from ClinicalTrials.gov. Nothing here was stated as a reason.
- 2026-02-23Phase 3 first posted: Regeneron Pharmaceuticals, Linvoseltamab + Bortezomib (NCT07428369)
- 2026-02-10Results posted on the registry: M.D. Anderson Cancer Center, Daratumumab (NCT03622775)
- 2026-02-06Phase 3 first posted: Regeneron Pharmaceuticals, Linvoseltamab + Daratumumab (NCT07393282)
- 2026-02-06Phase 3 first posted: AstraZeneca, AZD0120 + Daratumumab (NCT07391657)
- 2026-01-30Also stopped (terminated): Teva Branded Pharmaceutical Products R&D LLC, Modakafusp Alfa + Daratumumab (NCT05590377)
- 2026-01-29Also stopped (terminated): Teva Branded Pharmaceutical Products R&D LLC, Modakafusp alfa + Lenalidomide (NCT05556616)
- 2026-01-05Also stopped (terminated): Universitätsklinikum Hamburg-Eppendorf, Allogeneic Stem Cells + carfilzomib/lenalidomide/dexamethasone (KRD) (NCT05675319)
- 2025-12-23Results posted on the registry: Janssen Research & Development, LLC, Daratumumab SC: daratumumab + rHuPH20 (NCT03301220)
- 2025-12-16Phase 3 first posted: PrECOG, LLC., Arm A: Belantamab Mafodotin + Arm B: Daratumumab Hyaluronidase (NCT07285239)
- 2025-11-21Results posted on the registry: Thomas Jefferson University, Daratumumab and Hyaluronidase-fihj (NCT05511428)
- 2025-11-14Results posted on the registry: Sanofi, Isatuximab IV + Isatuximab SC (NCT05405166)
- 2025-11-04Also stopped (terminated): Incyte Corporation, INCB001158 + Daratumumab SC (NCT03837509)
- 2025-10-30Phase 3 first posted: Regeneron Pharmaceuticals, Linvoseltamab + Carfilzomib (NCT07222761)
- 2025-10-21Also stopped (terminated): University of California, San Diego, Ixazomib + Pomalidomide (NCT03590652)
- 2025-08-06Results posted on the registry: Teva Branded Pharmaceutical Products R&D LLC, Modakafusp Alfa + Daratumumab (NCT05590377)
- 2025-08-06Results posted on the registry: Teva Branded Pharmaceutical Products R&D LLC, Modakafusp alfa + Lenalidomide (NCT05556616)
- 2025-07-31Phase 3 first posted: AbbVie, Etentamig + Lenalidomide (NCT07095452)
- 2025-06-04Results posted on the registry: Mayo Clinic, Daratumumab + Dexamethasone (NCT03012880)
- 2025-05-20Results posted on the registry: Janssen Research & Development, LLC, Cilta-cel + Pomalidomide (NCT04181827)
- 2025-05-18Also stopped (terminated): Mayo Clinic, Belantamab Mafodotin + Daratumumab (NCT04892264)
- 2025-05-09Results posted on the registry: GlaxoSmithKline, Belantamab mafodotin + Daratumumab (NCT06868667)
- 2025-05-02Results posted on the registry: Gilead Sciences, Magrolimab + Daratumumab (NCT04892446)
- 2025-05-02Also stopped (terminated): Gilead Sciences, Magrolimab + Daratumumab (NCT04892446)
- 2025-05-01Phase 3 first posted: Celltrion, CT-P44(Daratumumab) + Darzalex Faspro(Daratumumab) (NCT06952478)
- 2025-04-23Results posted on the registry: GlaxoSmithKline, Belantamab mafodotin + Daratumumab (NCT06868654)
What is not public
- Internal portfolio and board discussions
- Unpublished trial data and interim analyses
- Terms of any partner or licence decision