Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT00991562 · ClinicalTrials.gov registry record · Phase 1
IMGN901 in Combination With Lenalidomide and Dexamethasone
A Phase 1 study, sponsored by ImmunoGen.
- Completed
- Registry status
- Phase 1
- Development phase
- 50
- Enrollment target
NCT00991562: Completed Phase 1 study, sponsored by ImmunoGen.
NCT00991562 is a Phase 1 study that has completed, run by ImmunoGen. The registered enrollment target is 50 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (17% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00991562, a Phase 1 study, has completed, sponsored by ImmunoGen.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 50 participants
- Enrollment target
Study Summary
The purpose of this study is to test IMGN901 in combination with lenalidomide and dexamethasone every 28 days.
Interventions
- DRUG IMGN901
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 50 participants |
| Start Date | 2009-12 |
| Est. Completion | 2014-10 |
| Phase | Phase 1 |
What the finished NCT00991562 record still lists
NCT00991562 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 50 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (17% lower).
The record links to 0 conditions, and to 1 intervention - of which IMGN901 is the first listed.
NCT00991562 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00991562 about?
NCT00991562 is a clinical study titled "IMGN901 in Combination With Lenalidomide and Dexamethasone". The purpose of this study is to test IMGN901 in combination with lenalidomide and dexamethasone every 28 days.
What is the current status of trial NCT00991562?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 50 participants. The study started on 2009-12. Estimated completion is 2014-10.
What interventions are being tested in trial NCT00991562?
The interventions under investigation include: IMGN901 (DRUG).
Who is sponsoring clinical trial NCT00991562?
This trial is sponsored by ImmunoGen, which has 15 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00991562's enrollment target sits among peer trials
50 973rd of 2000 higher than 984 of 2,000 other Phase 1 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
Nationwide trials with similar profiles
Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.
Similar enrollment target
- NCT00200889 · 50 participants · Early Phase 1
Mapping Auricular Vagus Nerve Circuitry
- NCT00409435 · 50 participants · Phase 2
A Study of Pyridostigmine in Postural Tachycardia Syndrome
- NCT01202305 · 50 participants
The Use of Lymph Node Biopsies to Support HIV Pathogenesis Studies
- NCT01225913 · 50 participants · Phase 4
Mechanism(s) of Airflow Limitation During Exacerbation of Asthma
Similar registry start date
- NCT05988463 · started 2027-01-01 · Phase 1
Dose-Escalation Study of Artesunate Patients With IPF
- NCT07219706 · started 2026-12-10 · NA
Dietary Fiber and Time Restricted Eating
- NCT02831335 · started 2026-12-01
Technical Development of Multi-Parametric Renocerebral MRI
- NCT05962346 · started 2026-12 · NA
Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia