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

NCT02944383 · ClinicalTrials.gov registry record · Phase 2

A 12-Week Study to Assess the Efficacy Safety and Tolerability of Gemcabene in Subjects With Severe Hypertriglyceridemia

A Phase 2 study, sponsored by NeuroBo Pharmaceuticals.

Completed
Registry status
Phase 2
Development phase
91
Enrollment target

NCT02944383: Completed Phase 2 study, sponsored by NeuroBo Pharmaceuticals.

NCT02944383 is a Phase 2 study that has completed, run by NeuroBo Pharmaceuticals. The registered enrollment target is 91 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (32% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT02944383, a Phase 2 study, has completed, sponsored by NeuroBo Pharmaceuticals.

COMPLETED
Registry status
Phase 2
Development phase
91 participants
Enrollment target

Study Summary

A 12-Week, Phase 2 Randomized, Double-Blind, Placebo-Controlled Study to Assess the Efficacy Safety and Tolerability of Gemcabene in Subjects with Severe Hypertriglyceridemia (INDIGO-1)

Primary Outcome

EOS was defined as the average of the week 10 and week 12 values. If either the week 10 or week 12 value was missing, then the single value (week 10 or week 12) was used. Completely missing values (both week 10 and week 12) were imputed using last observation carried forward (LOCF).

Interventions

  • DRUG Placebo
  • DRUG Gemcabene

Trial Details

FieldValue
Enrollment Target 91 participants
Start Date 2016-12
Est. Completion 2018-05-09
Phase Phase 2
NeuroBo Pharmaceuticals

8 total trials

What the finished NCT02944383 record still lists

NCT02944383 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 91 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (32% lower).

The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.

NCT02944383 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02944383 about?

NCT02944383 is a clinical study titled "A 12-Week Study to Assess the Efficacy Safety and Tolerability of Gemcabene in Subjects With Severe Hypertriglyceridemia". A 12-Week, Phase 2 Randomized, Double-Blind, Placebo-Controlled Study to Assess the Efficacy Safety and Tolerability of Gemcabene in Subjects with Severe Hypertriglyceridemia (INDIGO-1)

What is the current status of trial NCT02944383?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 91 participants. The study started on 2016-12. Estimated completion is 2018-05-09.

What interventions are being tested in trial NCT02944383?

The interventions under investigation include: Placebo (DRUG), Gemcabene (DRUG).

Who is sponsoring clinical trial NCT02944383?

This trial is sponsored by NeuroBo Pharmaceuticals, which has 8 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02944383's enrollment target sits among peer trials

91 771st of 2000 higher than 1,229 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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

  • NCT02671448 · 91 participants · NA

    Pilot Trial of Homebound Stem Cell Transplantation

  • NCT04835857 · 91 participants

    Comparison of Cuff-Less Wrist Wearable Blood Pressure Device to Cuff Based Blood Pressure Measuring Devices

  • NCT05184842 · 91 participants · Phase 2

    Metabolically Optimized, Non-cytotoxic Low Dose Weekly Decitabine/Venetoclax in MDS and AML

  • NCT05685173 · 91 participants · Phase 1

    A Trial to Study if REGN5837 in Combination With Odronextamab is Safe for Adult Participants With Aggressive B-cell Non-Hodgkin Lymphomas

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 NCT02944383, the US trial registry maintained by the National Library of Medicine. NCT02944383 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.