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NCT01609816 · ClinicalTrials.gov registry record · Phase 1

Dasatinib for Modulating Immune System After Autologous Stem Cell Transplants for Multiple Myeloma, Non-Hodgkin, or Hodgkin Lymphoma

A Phase 1 study, sponsored by Barbara Ann Karmanos Cancer Institute.

Terminated
Registry status
Phase 1
Development phase
8
Enrollment target

NCT01609816: Clinical Trial Phase 1 study, sponsored by Barbara Ann Karmanos Cancer Institute.

NCT01609816 is a Phase 1 study that was terminated before completion, run by Barbara Ann Karmanos Cancer Institute. The registered enrollment target is 8 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (87% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01609816, a Phase 1 study, was terminated before completion, sponsored by Barbara Ann Karmanos Cancer Institute.

TERMINATED
Registry status
Phase 1
Development phase
8 participants
Enrollment target

Study Summary

This study uses a drug called dasatinib to produce an anti-cancer effect called large granular lymphocyte cellular expansion. Large granular lymphocytes are blood cells known as natural killer cells that remove cancer cells. Researchers think that dasatinib may cause large granular lymphocyte expansion to happen in patients who have received a blood stem cell transplant (SCT) between 3 to 15 months after the blood SCT. In this research study, researchers want to find how well dasatinib can be tolerated, the best dose to take of dasatinib and to estimate how often large granular lymphocytic cellular expansion happens at the best dose of dasatinib.

Interventions

  • DRUG Dasatinib

Trial Details

FieldValue
Enrollment Target 8 participants
Start Date 2015-02-12
Est. Completion 2018-10-09
Phase Phase 1

Why NCT01609816 stopped before completion

NCT01609816 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 8 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (87% lower).

The record links to 0 conditions, and to 1 intervention - of which Dasatinib is the first listed.

NCT01609816 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01609816 about?

NCT01609816 is a clinical study titled "Dasatinib for Modulating Immune System After Autologous Stem Cell Transplants for Multiple Myeloma, Non-Hodgkin, or Hodgkin Lymphoma". This study uses a drug called dasatinib to produce an anti-cancer effect called large granular lymphocyte cellular expansion. Large granular lymphocytes are blood cells known as natural killer cells that remove cancer cells. Researchers think that dasatinib may cause large granular lymphocyte expans...

What is the current status of trial NCT01609816?

This trial is currently terminated. It is a Phase 1 study. The enrollment target is 8 participants. The study started on 2015-02-12. Estimated completion is 2018-10-09.

What interventions are being tested in trial NCT01609816?

The interventions under investigation include: Dasatinib (DRUG).

Who is sponsoring clinical trial NCT01609816?

This trial is sponsored by Barbara Ann Karmanos Cancer Institute, which has 139 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01609816's enrollment target sits among peer trials

8 1959th of 2000 higher than 29 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

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Source: ClinicalTrials.gov NCT01609816, the US trial registry maintained by the National Library of Medicine. NCT01609816 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.