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NCT07615010 · ClinicalTrials.gov registry record · Phase 2

A Clinical Trial to Evaluate agenT-797 Plus Standard of Care in Participants With Severe Pneumonia With Moderate to Severe Acute Hypoxemic Respiratory Failure

A Phase 2 study, sponsored by MiNK Therapeutics.

Recruiting
Registry status
Phase 2
Development phase
90
Enrollment target

NCT07615010 is a Phase 2 study that is actively recruiting participants, run by MiNK Therapeutics. The registered enrollment target is 90 participants.

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The verdict

NCT07615010, a Phase 2 study, is actively recruiting participants, sponsored by MiNK Therapeutics.

RECRUITING
Registry status
Phase 2
Development phase
90 participants
Enrollment target

Study Summary

This clinical trial will evaluate the efficacy and safety of a single intravenous dose of agenT-797 administered in addition to standard of care (SOC), compared with placebo plus SOC, in reducing short-term mortality in adult participants with severe pneumonia and moderate to severe AHRF. All participants will receive SOC management for severe pneumonia and acute respiratory distress syndrome (ARDS).

Interventions

  • DRUG Placebo
  • DRUG Standard of Care (SOC)
  • DRUG agenT-797

Trial Details

FieldValue
Enrollment Target 90 participants
Start Date 2026-05-26
Est. Completion 2027-08
Phase Phase 2

Sponsor

MiNK Therapeutics

4 total trials

What the Registry Record Tells You About NCT07615010

The ClinicalTrials.gov registry entry for NCT07615010 describes a study currently listed as recruiting, categorized as Phase 2. The registered enrollment target is 90 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is MiNK Therapeutics, which has 4 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 3 interventions - of which Placebo is the first listed.

NCT07615010 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT07615010 about?

NCT07615010 is a clinical study titled "A Clinical Trial to Evaluate agenT-797 Plus Standard of Care in Participants With Severe Pneumonia With Moderate to Severe Acute Hypoxemic Respiratory Failure". This clinical trial will evaluate the efficacy and safety of a single intravenous dose of agenT-797 administered in addition to standard of care (SOC), compared with placebo plus SOC, in reducing short-term mortality in adult participants with severe pneumonia and moderate to severe AHRF. All partic...

What is the current status of trial NCT07615010?

This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 90 participants. The study started on 2026-05-26. Estimated completion is 2027-08.

What interventions are being tested in trial NCT07615010?

The interventions under investigation include: Placebo (DRUG), Standard of Care (SOC) (DRUG), agenT-797 (DRUG).

Who is sponsoring clinical trial NCT07615010?

This trial is sponsored by MiNK Therapeutics, which has 4 total clinical trials registered on ClinicalTrials.gov.

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

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