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NCT02845297 · ClinicalTrials.gov registry record · Phase 2

Study of Azacitidine in Combination With Pembrolizumab in R/R AML Patients and in Newly Diagnosed Older Patients

A Phase 2 study, sponsored by Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins.

Completed
Registry status
Phase 2
Development phase
67
Enrollment target

NCT02845297 is a Phase 2 study that has completed, run by Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins. The registered enrollment target is 67 participants.

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The verdict

NCT02845297, a Phase 2 study, has completed, sponsored by Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins.

COMPLETED
Registry status
Phase 2
Development phase
67 participants
Enrollment target

Study Summary

This is a multicenter, nonrandomized, open-label phase 2 study (with a safety run-in phase) of azacitidine (AZA) 75 mg/m2 given IV or SQ on days 1-7 every 28 days in combination with pembrolizumab 200 mg given IV every 3 weeks (starting on day 8 of cycle 1). The dose/schedule of AZA selected for this study is FDA approved for patients with MDS/AML.

Interventions

  • DRUG pembrolizumab
  • DRUG Azacitadine

Trial Details

FieldValue
Enrollment Target 67 participants
Start Date 2016-07
Est. Completion 2022-12
Phase Phase 2

What the Registry Record Tells You About NCT02845297

The ClinicalTrials.gov registry entry for NCT02845297 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 67 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins, which has 523 total studies on file at ClinicalTrials.gov.

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

NCT02845297 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT02845297 about?

NCT02845297 is a clinical study titled "Study of Azacitidine in Combination With Pembrolizumab in R/R AML Patients and in Newly Diagnosed Older Patients". This is a multicenter, nonrandomized, open-label phase 2 study (with a safety run-in phase) of azacitidine (AZA) 75 mg/m2 given IV or SQ on days 1-7 every 28 days in combination with pembrolizumab 200 mg given IV every 3 weeks (starting on day 8 of cycle 1). The dose/schedule of AZA selected for thi...

What is the current status of trial NCT02845297?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 67 participants. The study started on 2016-07. Estimated completion is 2022-12.

What interventions are being tested in trial NCT02845297?

The interventions under investigation include: pembrolizumab (DRUG), Azacitadine (DRUG).

Who is sponsoring clinical trial NCT02845297?

This trial is sponsored by Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins, which has 523 total clinical trials registered on ClinicalTrials.gov.

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

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.