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COMPLETED Phase 2

A Study to Evaluate the Efficacy, Safety, and Tolerability of CBL-514 Injection for Reducing Subcutaneous Fat (Stage 2)

NCT04897412 · View on ClinicalTrials.gov ↗

Study Summary

The Stage 2 of this phase 2 study will be a randomized, single-blind, placebo-controlled, parallel, and multiple-dose study to assess the efficacy, safety, and subject satisfaction of CBL-514.

Conditions Studied

Interventions

  • OTHER Placebo
  • DRUG CBL-514 Injection

Study Locations (5)

Illinois

  • Investigational site 1 — Chicago

Nebraska

  • Investigational site 2 — Omaha

Tennessee

  • Investigational site 3 — Nashville

Texas

  • Investigational site 4 — Austin

Victoria

  • Investigational site 5 — Melbourne

Trial Details

FieldValue
Enrollment Target 75 participants
Start Date 2022-02-14
Est. Completion 2023-03-22
Phase Phase 2

Sponsor

Caliway Biopharmaceuticals Co.

3 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT04897412

The ClinicalTrials.gov registry entry for NCT04897412 describes a study currently listed as completed. 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 75 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Caliway Biopharmaceuticals Co., which has 3 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 Subcutaneous Fat appearing as the primary indexed condition, and to 2 interventions — of which Placebo 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: NCT04897412 reports 5 study locations spanning 5 distinct geographic areas — top geographies include Illinois, Nebraska, Tennessee. 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 NCT04897412 about?

NCT04897412 is a clinical study titled "A Study to Evaluate the Efficacy, Safety, and Tolerability of CBL-514 Injection for Reducing Subcutaneous Fat (Stage 2)". The Stage 2 of this phase 2 study will be a randomized, single-blind, placebo-controlled, parallel, and multiple-dose study to assess the efficacy, safety, and subject satisfaction of CBL-514.

What is the current status of trial NCT04897412?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 75 participants. The study started on 2022-02-14. Estimated completion is 2023-03-22.

What conditions does trial NCT04897412 study?

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

What interventions are being tested in trial NCT04897412?

The interventions under investigation include: Placebo (OTHER), CBL-514 Injection (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT04897412?

This trial is sponsored by Caliway Biopharmaceuticals Co., which has 3 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT04897412 being conducted?

This trial has 5 study locations across Illinois, Nebraska, Tennessee, Texas, Victoria. 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