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NCT03006237 · ClinicalTrials.gov registry record · Phase 1

IS-001 Injection Phase-1 Safety, Tolerance and Pharmacokinetics

A Phase 1 study, sponsored by Intuitive Surgical.

Completed
Registry status
Phase 1
Development phase
24
Enrollment target

NCT03006237: Completed Phase 1 study, sponsored by Intuitive Surgical.

NCT03006237 is a Phase 1 study that has completed, run by Intuitive Surgical. The registered enrollment target is 24 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (60% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03006237, a Phase 1 study, has completed, sponsored by Intuitive Surgical.

COMPLETED
Registry status
Phase 1
Development phase
24 participants
Enrollment target

Study Summary

A Phase 1 Open Label Single Center Safety, Tolerability and Pharmacokinetic Study of IS-001

Primary Outcome

Vital signs, 12-lead ECG, serum chemistry (CMP) and hematology (CBC), urinalysis and incidence of treatment-emergent adverse events

Interventions

  • DRUG IS-001
  • DEVICE da Vinci® Si/Xi Surgical System

Trial Details

FieldValue
Enrollment Target 24 participants
Start Date 2016-12
Est. Completion 2017-12
Phase Phase 1
Intuitive Surgical

40 total trials

What the finished NCT03006237 record still lists

NCT03006237 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 24 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (60% lower).

The record links to 0 conditions, and to 2 interventions - of which IS-001 is the first listed.

NCT03006237 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03006237 about?

NCT03006237 is a clinical study titled "IS-001 Injection Phase-1 Safety, Tolerance and Pharmacokinetics". A Phase 1 Open Label Single Center Safety, Tolerability and Pharmacokinetic Study of IS-001

What is the current status of trial NCT03006237?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 24 participants. The study started on 2016-12. Estimated completion is 2017-12.

What interventions are being tested in trial NCT03006237?

The interventions under investigation include: IS-001 (DRUG), da Vinci® Si/Xi Surgical System (DEVICE).

Who is sponsoring clinical trial NCT03006237?

This trial is sponsored by Intuitive Surgical, which has 40 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03006237's enrollment target sits among peer trials

24 1520th of 2000 higher than 405 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 NCT03006237, the US trial registry maintained by the National Library of Medicine. NCT03006237 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.