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NCT01396200 · ClinicalTrials.gov registry record · Early Phase 1

Cyclophosphamide and Pulse Dexamethasone With Rapamycin or Hydroxychloroquine

A Early Phase 1 study, sponsored by Abramson Cancer Center at Penn Medicine.

Completed
Registry status
Early Phase 1
Development phase
6
Enrollment target

NCT01396200 is a Early Phase 1 study that has completed, run by Abramson Cancer Center at Penn Medicine. The registered enrollment target is 6 participants.

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The verdict

NCT01396200, a Early Phase 1 study, has completed, sponsored by Abramson Cancer Center at Penn Medicine.

COMPLETED
Registry status
Early Phase 1
Development phase
6 participants
Enrollment target

Study Summary

The purpose of this study is to determine the feasibility of giving (i) rapamycin or (ii) hydroxychloroquine (HCQ), with standard doses of infusional cyclophosphamide and pulse dexamethasone (cy/dex) for patients with relapsed/refractory multiple myeloma, as well as the feasibility of obtaining multiple blood and bone marrow samples during treatment to assess the pharmacodynamic effects of the treatment.

Interventions

  • DRUG Rapamycin
  • DRUG Hydroxychloroquine

Trial Details

FieldValue
Enrollment Target 6 participants
Start Date 2011-06
Est. Completion 2012-10
Phase Early Phase 1

What the Registry Record Tells You About NCT01396200

The ClinicalTrials.gov registry entry for NCT01396200 describes a study currently listed as completed, categorized as Early Phase 1. The registered enrollment target is 6 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Abramson Cancer Center at Penn Medicine, which has 402 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which Rapamycin is the first listed.

NCT01396200 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT01396200 about?

NCT01396200 is a clinical study titled "Cyclophosphamide and Pulse Dexamethasone With Rapamycin or Hydroxychloroquine". The purpose of this study is to determine the feasibility of giving (i) rapamycin or (ii) hydroxychloroquine (HCQ), with standard doses of infusional cyclophosphamide and pulse dexamethasone (cy/dex) for patients with relapsed/refractory multiple myeloma, as well as the feasibility of obtaining mult...

What is the current status of trial NCT01396200?

This trial is currently completed. It is a Early Phase 1 study. The enrollment target is 6 participants. The study started on 2011-06. Estimated completion is 2012-10.

What interventions are being tested in trial NCT01396200?

The interventions under investigation include: Rapamycin (DRUG), Hydroxychloroquine (DRUG).

Who is sponsoring clinical trial NCT01396200?

This trial is sponsored by Abramson Cancer Center at Penn Medicine, which has 402 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.