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NCT05227144 · ClinicalTrials.gov registry record · Phase 1

Study of ORIC-533 in Relapsed or Refractory Multiple Myeloma

A Phase 1 study, sponsored by ORIC Pharmaceuticals.

Completed
Registry status
Phase 1
Development phase
31
Enrollment target

NCT05227144: Completed Phase 1 study, sponsored by ORIC Pharmaceuticals.

NCT05227144 is a Phase 1 study that has completed, run by ORIC Pharmaceuticals. The registered enrollment target is 31 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (48% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05227144, a Phase 1 study, has completed, sponsored by ORIC Pharmaceuticals.

COMPLETED
Registry status
Phase 1
Development phase
31 participants
Enrollment target

Study Summary

The purpose of this study is to establish the Recommended Phase 2 Dose (RP2D), safety, pharmacokinetics (PK), pharmacodynamics (PD), and preliminary antimyeloma activity of ORIC-533 in patients with multiple myeloma who have exhausted available treatment options

Primary Outcome

RP2D as determined by interval 3+3 dose escalation design

Interventions

  • DRUG ORIC-533

Trial Details

FieldValue
Enrollment Target 31 participants
Start Date 2022-01-06
Est. Completion 2025-03-03
Phase Phase 1
ORIC Pharmaceuticals

7 total trials

What the finished NCT05227144 record still lists

NCT05227144 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 31 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (48% lower).

The record links to 0 conditions, and to 1 intervention - of which ORIC-533 is the first listed.

NCT05227144 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT05227144 about?

NCT05227144 is a clinical study titled "Study of ORIC-533 in Relapsed or Refractory Multiple Myeloma". The purpose of this study is to establish the Recommended Phase 2 Dose (RP2D), safety, pharmacokinetics (PK), pharmacodynamics (PD), and preliminary antimyeloma activity of ORIC-533 in patients with multiple myeloma who have exhausted available treatment options

What is the current status of trial NCT05227144?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 31 participants. The study started on 2022-01-06. Estimated completion is 2025-03-03.

What interventions are being tested in trial NCT05227144?

The interventions under investigation include: ORIC-533 (DRUG).

Who is sponsoring clinical trial NCT05227144?

This trial is sponsored by ORIC Pharmaceuticals, which has 7 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT05227144's enrollment target sits among peer trials

31 1322nd of 2000 higher than 669 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 NCT05227144, the US trial registry maintained by the National Library of Medicine. NCT05227144 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.