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NCT01356173 · ClinicalTrials.gov registry record · Phase 1

Evaluating the Safety and Tolerability of GDC-0349 in Patients With Locally Advanced or Metastatic Solid Tumors or Non Hodgkin's Lymphoma

A Phase 1 study, sponsored by Genentech.

Completed
Registry status
Phase 1
Development phase
10
Enrollment target

NCT01356173: Completed Phase 1 study, sponsored by Genentech.

NCT01356173 is a Phase 1 study that has completed, run by Genentech. The registered enrollment target is 10 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (83% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01356173, a Phase 1 study, has completed, sponsored by Genentech.

COMPLETED
Registry status
Phase 1
Development phase
10 participants
Enrollment target

Study Summary

This is an open-label, multicenter, Phase I, dose-escalation study to assess the safety, tolerability, and pharmacokinetic (PK) of GDC-0349 administered once daily (QD), orally (PO).

Interventions

  • DRUG GDC-0349

Trial Details

FieldValue
Enrollment Target 10 participants
Start Date 2011-06
Est. Completion 2012-12
Phase Phase 1
Genentech

332 total trials

What the finished NCT01356173 record still lists

NCT01356173 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 10 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (83% lower).

The record links to 0 conditions, and to 1 intervention - of which GDC-0349 is the first listed.

NCT01356173 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01356173 about?

NCT01356173 is a clinical study titled "Evaluating the Safety and Tolerability of GDC-0349 in Patients With Locally Advanced or Metastatic Solid Tumors or Non Hodgkin's Lymphoma". This is an open-label, multicenter, Phase I, dose-escalation study to assess the safety, tolerability, and pharmacokinetic (PK) of GDC-0349 administered once daily (QD), orally (PO).

What is the current status of trial NCT01356173?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 10 participants. The study started on 2011-06. Estimated completion is 2012-12.

What interventions are being tested in trial NCT01356173?

The interventions under investigation include: GDC-0349 (DRUG).

Who is sponsoring clinical trial NCT01356173?

This trial is sponsored by Genentech, which has 332 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01356173's enrollment target sits among peer trials

10 1913th of 2000 higher than 46 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 NCT01356173, the US trial registry maintained by the National Library of Medicine. NCT01356173 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.