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NCT01679028 · ClinicalTrials.gov registry record · Phase 1

Dose-Escalate Study to Investigate the Safety and Tolerability of T89 in Japanese

A Phase 1 study, sponsored by Tasly Pharmaceuticals.

Completed
Registry status
Phase 1
Development phase
20
Enrollment target

NCT01679028: Completed Phase 1 study, sponsored by Tasly Pharmaceuticals.

NCT01679028 is a Phase 1 study that has completed, run by Tasly Pharmaceuticals. The registered enrollment target is 20 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (67% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01679028, a Phase 1 study, has completed, sponsored by Tasly Pharmaceuticals.

COMPLETED
Registry status
Phase 1
Development phase
20 participants
Enrollment target

Study Summary

The purpose of this study is to see how safe an investigational new drug (T89) is and how well healthy Japanese subjects tolerate it when given two single doses and a multiple dose.

Primary Outcome

the Incidence of Adverse Drug Events and serious adverse events

Interventions

  • DRUG T89 Group A
  • DRUG Placebo Group A
  • DRUG Placebo Group B
  • DRUG T89 Group B
  • DRUG Placebo Group C

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2012-08
Est. Completion 2013-02
Phase Phase 1
Tasly Pharmaceuticals

8 total trials

What the finished NCT01679028 record still lists

NCT01679028 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 20 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (67% lower).

The record links to 0 conditions, and to 5 interventions - of which T89 Group A is the first listed.

NCT01679028 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01679028 about?

NCT01679028 is a clinical study titled "Dose-Escalate Study to Investigate the Safety and Tolerability of T89 in Japanese". The purpose of this study is to see how safe an investigational new drug (T89) is and how well healthy Japanese subjects tolerate it when given two single doses and a multiple dose.

What is the current status of trial NCT01679028?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 20 participants. The study started on 2012-08. Estimated completion is 2013-02.

What interventions are being tested in trial NCT01679028?

The interventions under investigation include: T89 Group A (DRUG), Placebo Group A (DRUG), Placebo Group B (DRUG), T89 Group B (DRUG), Placebo Group C (DRUG).

Who is sponsoring clinical trial NCT01679028?

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

How this trial's enrollment target compares

Where NCT01679028's enrollment target sits among peer trials

20 1629th of 2000 higher than 285 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 NCT01679028, the US trial registry maintained by the National Library of Medicine. NCT01679028 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.