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NCT05091866 · ClinicalTrials.gov registry record · Early Phase 1

Natural Progesterone for the Treatment of Recurrent Glioblastoma

A Early Phase 1 study of Recurrent Glioblastoma and Gliosarcoma, sponsored by Emory University.

Active
Registry status
Early Phase 1
Development phase
4
Enrollment target
1
Study location

NCT05091866 is a Early Phase 1 study of Recurrent Glioblastoma and Gliosarcoma that is active but no longer recruiting, run by Emory University. The registered enrollment target is 4 participants, below the 69-participant average among 62 other Recurrent Glioblastoma trials with a reported enrollment target (94% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT05091866, a Early Phase 1 study of Recurrent Glioblastoma and Gliosarcoma, is active but no longer recruiting, sponsored by Emory University.

ACTIVE NOT RECRUITING
Registry status
Early Phase 1
Development phase
4 participants
Enrollment target
1
Study location

Study Summary

This early phase I trial identifies the best dose, possible benefits and/or side effects of natural progesterone in treating patients with glioblastoma that has come back (recurrent). Progesterone is a type of hormone made by the body that plays a role in the menstrual cycle and pregnancy. Progesterone may help control tumor growth and spread in patients with glioblastoma.

Interventions

  • OTHER Quality-of-Life Assessment
  • OTHER Questionnaire Administration
  • BIOLOGICAL Therapeutic Progesterone

Study Locations (1)

Georgia

  • Emory University Hospital/Winship Cancer Institute - Atlanta

Trial Details

FieldValue
Enrollment Target 4 participants
Start Date 2022-04-11
Est. Completion 2027-04-01
Phase Early Phase 1

Sponsor

Emory University

1,208 total trials

What the Registry Record Tells You About NCT05091866

The ClinicalTrials.gov registry entry for NCT05091866 describes a study currently listed as active not recruiting, categorized as Early Phase 1. The registered enrollment target is 4 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 69-participant average among 62 other Recurrent Glioblastoma trials with a reported enrollment target (94% lower). The listed sponsor is Emory University, which has 1,208 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Recurrent Glioblastoma appearing as the primary indexed condition, and to 3 interventions - of which Quality-of-Life Assessment is the first listed.

NCT05091866 reports 1 study location spanning 1 distinct geographic area - top geographies include Georgia.

Frequently Asked Questions

What is clinical trial NCT05091866 about?

NCT05091866 is a clinical study titled "Natural Progesterone for the Treatment of Recurrent Glioblastoma". This early phase I trial identifies the best dose, possible benefits and/or side effects of natural progesterone in treating patients with glioblastoma that has come back (recurrent). Progesterone is a type of hormone made by the body that plays a role in the menstrual cycle and pregnancy. Progester...

What is the current status of trial NCT05091866?

This trial is currently active not recruiting. It is a Early Phase 1 study. The enrollment target is 4 participants. The study started on 2022-04-11. Estimated completion is 2027-04-01.

What conditions does trial NCT05091866 study?

This clinical trial studies the following conditions: Recurrent Glioblastoma, Gliosarcoma.

What interventions are being tested in trial NCT05091866?

The interventions under investigation include: Quality-of-Life Assessment (OTHER), Questionnaire Administration (OTHER), Therapeutic Progesterone (BIOLOGICAL).

Who is sponsoring clinical trial NCT05091866?

This trial is sponsored by Emory University, which has 1,208 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05091866 being conducted?

This trial has 1 study location across Georgia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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

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