Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT07549698 · ClinicalTrials.gov registry record · Phase 1

Safety and Preliminary Efficacy of CTX112 in Adult Participants With Relapsed/Refractory Hematologic Autoimmune Disease

A Phase 1 study, sponsored by CRISPR Therapeutics.

Recruiting
Registry status
Phase 1
Development phase
60
Enrollment target

NCT07549698: Recruiting Phase 1 study, sponsored by CRISPR Therapeutics.

NCT07549698 is a Phase 1 study that is actively recruiting participants, run by CRISPR Therapeutics. The registered enrollment target is 60 participants, roughly in line with the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT07549698, a Phase 1 study, is actively recruiting participants, sponsored by CRISPR Therapeutics.

RECRUITING
Registry status
Phase 1
Development phase
60 participants
Enrollment target

Study Summary

This is a single-arm, open-label, multicenter, ascending dose Phase 1/2 trial evaluating the safety and preliminary efficacy of CTX112 or Zugocabtagene geleucel (zugo-cel) in adult participants with relapsed/refractory primary Immune Thrombocytopenia (ITP) and relapsed/refractory primary Warm Autoimmune Hemolytic Anemia (wAIHA).

Primary Outcome

Incidence of dose-limiting toxicities.

Interventions

  • BIOLOGICAL CTX112

Trial Details

FieldValue
Enrollment Target 60 participants
Start Date 2026-06
Est. Completion 2033-12
Phase Phase 1
CRISPR Therapeutics

10 total trials

What NCT07549698 shows while recruiting

NCT07549698 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 60 participants, a relatively small participant target, roughly in line with the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target.

The record links to 0 conditions, and to 1 intervention - of which CTX112 is the first listed.

NCT07549698 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT07549698 about?

NCT07549698 is a clinical study titled "Safety and Preliminary Efficacy of CTX112 in Adult Participants With Relapsed/Refractory Hematologic Autoimmune Disease". This is a single-arm, open-label, multicenter, ascending dose Phase 1/2 trial evaluating the safety and preliminary efficacy of CTX112 or Zugocabtagene geleucel (zugo-cel) in adult participants with relapsed/refractory primary Immune Thrombocytopenia (ITP) and relapsed/refractory primary Warm Autoim...

What is the current status of trial NCT07549698?

This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 60 participants. The study started on 2026-06. Estimated completion is 2033-12.

What interventions are being tested in trial NCT07549698?

The interventions under investigation include: CTX112 (BIOLOGICAL).

Who is sponsoring clinical trial NCT07549698?

This trial is sponsored by CRISPR Therapeutics, which has 10 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT07549698's enrollment target sits among peer trials

60 831st of 2000 higher than 1,106 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

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT00576069 · 60 participants

    Mechanism(s)of Airflow Limitation in Moderate-severe Persistent Asthma

  • NCT01297400 · 60 participants · Phase 2

    Phase 2 Pilot Study of the Safety and Efficacy of Topical MW-III in Thermal Burns

  • NCT01734122 · 60 participants

    Stereotactic Radiosurgery for Essential Tremor and Parkinsonian Tremor

  • NCT01804634 · 60 participants · Phase 2

    Reduced Intensity Haploidentical BMT for High Risk Solid Tumors

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT07549698, the US trial registry maintained by the National Library of Medicine. NCT07549698 (small enrollment · none site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.