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NCT05950334 · ClinicalTrials.gov registry record · Phase 1

FT522 With Rituximab in Relapsed/Refractory B-Cell Lymphoma (FT522-101)

A Phase 1 study, sponsored by Fate Therapeutics.

Completed
Registry status
Phase 1
Development phase
20
Enrollment target

NCT05950334 is a Phase 1 study that has completed, run by Fate Therapeutics. The registered enrollment target is 20 participants.

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The verdict

NCT05950334, a Phase 1 study, has completed, sponsored by Fate Therapeutics.

COMPLETED
Registry status
Phase 1
Development phase
20 participants
Enrollment target

Study Summary

This is a phase 1 study of FT522 administered with rituximab in participants with relapsed/refractory B-cell lymphoma (R/R BCL). The primary objectives of the study are to evaluate the safety and tolerability of FT522 in combination with rituximab, and to determine the recommended phase 2 dose (RP2D) of FT522 in combination with rituximab; each objective will be assessed with or without conditioning chemotherapy.

Interventions

  • DRUG Cyclophosphamide
  • DRUG Fludarabine
  • DRUG Rituximab
  • DRUG Bendamustine
  • DRUG FT522

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2023-11-16
Est. Completion 2025-06-30
Phase Phase 1

Sponsor

Fate Therapeutics

22 total trials

What the Registry Record Tells You About NCT05950334

The ClinicalTrials.gov registry entry for NCT05950334 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 20 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Fate Therapeutics, which has 22 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 5 interventions - of which Cyclophosphamide is the first listed.

NCT05950334 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT05950334 about?

NCT05950334 is a clinical study titled "FT522 With Rituximab in Relapsed/Refractory B-Cell Lymphoma (FT522-101)". This is a phase 1 study of FT522 administered with rituximab in participants with relapsed/refractory B-cell lymphoma (R/R BCL). The primary objectives of the study are to evaluate the safety and tolerability of FT522 in combination with rituximab, and to determine the recommended phase 2 dose (RP2D...

What is the current status of trial NCT05950334?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 20 participants. The study started on 2023-11-16. Estimated completion is 2025-06-30.

What interventions are being tested in trial NCT05950334?

The interventions under investigation include: Cyclophosphamide (DRUG), Fludarabine (DRUG), Rituximab (DRUG), Bendamustine (DRUG), FT522 (DRUG).

Who is sponsoring clinical trial NCT05950334?

This trial is sponsored by Fate Therapeutics, which has 22 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.