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NCT00728936 · ClinicalTrials.gov registry record · Phase 1

Placebo-controlled, Dose-escalation Study of the Safety of IMO-2125 (Immunomodulatory Oligonucleotide) in Hepatitis C-infected Patients

A Phase 1 study, sponsored by Idera Pharmaceuticals.

Completed
Registry status
Phase 1
Development phase
58
Enrollment target

NCT00728936: Completed Phase 1 study, sponsored by Idera Pharmaceuticals.

NCT00728936 is a Phase 1 study that has completed, run by Idera Pharmaceuticals. The registered enrollment target is 58 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.

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The verdict

NCT00728936, a Phase 1 study, has completed, sponsored by Idera Pharmaceuticals.

COMPLETED
Registry status
Phase 1
Development phase
58 participants
Enrollment target

Study Summary

First-in-humans, phase 1, dose-escalation study with 4 dose levels of single-agent IMO-2125.

Primary Outcome

Count and percentage of subjects with treatment emergent adverse events

Interventions

  • DRUG Saline placebo
  • DRUG IMO-2125

Trial Details

FieldValue
Enrollment Target 58 participants
Start Date 2007-09
Est. Completion 2010-05
Phase Phase 1
Idera Pharmaceuticals

10 total trials

What the finished NCT00728936 record still lists

NCT00728936 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 58 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 2 interventions - of which Saline placebo is the first listed.

NCT00728936 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00728936 about?

NCT00728936 is a clinical study titled "Placebo-controlled, Dose-escalation Study of the Safety of IMO-2125 (Immunomodulatory Oligonucleotide) in Hepatitis C-infected Patients". First-in-humans, phase 1, dose-escalation study with 4 dose levels of single-agent IMO-2125.

What is the current status of trial NCT00728936?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 58 participants. The study started on 2007-09. Estimated completion is 2010-05.

What interventions are being tested in trial NCT00728936?

The interventions under investigation include: Saline placebo (DRUG), IMO-2125 (DRUG).

Who is sponsoring clinical trial NCT00728936?

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

How this trial's enrollment target compares

Where NCT00728936's enrollment target sits among peer trials

58 895th of 2000 higher than 1,100 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

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Source: ClinicalTrials.gov NCT00728936, the US trial registry maintained by the National Library of Medicine. NCT00728936 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.