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ACTIVE NOT RECRUITING Phase 2

A Study to Evaluate the Long-Term Safety and Efficacy of Paltusotine for the Treatment of Acromegaly (ACROBAT Advance)

NCT04261712 · View on ClinicalTrials.gov ↗

Study Summary

A phase 2, open label, long-term extension study designed to evaluate the safety and efficacy of paltusotine (formerly CRN00808; an oral selective nonpeptide somatostatin receptor type 2 biased agonist) in subjects with acromegaly.

Conditions Studied

Interventions

  • DRUG Paltusotine

Study Locations (20)

Other

  • Crinetics Study Site — Rio de Janeiro
  • Crinetics Study Site — Rio de Janeiro
  • Crinetics Study Site — São Paulo
  • Crinetics Study Site — München
  • Crinetics Study Site — Athens
  • Crinetics Study Site 1 — Athens
  • Crinetics Study Site 2 — Athens
  • Crinetics Study Site — Thessaloniki
  • Crinetics Study Site — Budapest
  • Crinetics Study Site — Budapest
  • Crinetics Study Site — Pécs
  • Crinetics Study Site — Belgrade

Pennsylvania

  • Crinetics Study Site — Pittsburgh
  • Crinetics Study Site — Pittsburgh

California

  • Crinetics Study Site — Los Angeles

Illinois

  • Crinetics Study Site — Chicago

Massachusetts

  • Crinetics Study Site — Boston

Ohio

  • Crinetics Study Site — Columbus

Texas

  • Crinetics Study Site — Dallas

Paraná

  • Crinetics Study Site — Curitiba

Trial Details

FieldValue
Enrollment Target 43 participants
Start Date 2020-01-29
Est. Completion 2028-03
Phase Phase 2

Sponsor

Crinetics Pharmaceuticals

9 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT04261712

The ClinicalTrials.gov registry entry for NCT04261712 describes a study currently listed as active not recruiting. It is categorized as Phase 2, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 43 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Crinetics Pharmaceuticals, which has 9 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Acromegaly appearing as the primary indexed condition, and to 1 intervention — of which Paltusotine is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT04261712 reports 20 study locations spanning 8 distinct geographic areas — top geographies include Other, Pennsylvania, California. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT04261712 about?

NCT04261712 is a clinical study titled "A Study to Evaluate the Long-Term Safety and Efficacy of Paltusotine for the Treatment of Acromegaly (ACROBAT Advance)". A phase 2, open label, long-term extension study designed to evaluate the safety and efficacy of paltusotine (formerly CRN00808; an oral selective nonpeptide somatostatin receptor type 2 biased agonist) in subjects with acromegaly.

What is the current status of trial NCT04261712?

This trial is currently active not recruiting. It is a Phase 2 study. The enrollment target is 43 participants. The study started on 2020-01-29. Estimated completion is 2028-03.

What conditions does trial NCT04261712 study?

This clinical trial studies the following conditions: Acromegaly. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT04261712?

The interventions under investigation include: Paltusotine (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT04261712?

This trial is sponsored by Crinetics Pharmaceuticals, which has 9 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT04261712 being conducted?

This trial has 20 study locations across California, Illinois, Massachusetts, Ohio, Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

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