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

NCT00606814 · ClinicalTrials.gov registry record · Phase 1

Phase I Study of IPI-504 and Docetaxel in Patients With Advanced Solid Tumors

A Phase 1 study of Solid Tumors, sponsored by Infinity Pharmaceuticals.

Completed
Registry status
Phase 1
Development phase
60
Enrollment target
8
Study locations

NCT00606814: Completed Phase 1 study of Solid Tumors, sponsored by Infinity Pharmaceuticals.

NCT00606814 is a Phase 1 study of Solid Tumors that has completed, run by Infinity Pharmaceuticals. The registered enrollment target is 60 participants, below the 284-participant average among 125 other Solid Tumors trials with a reported enrollment target (79% lower). The trial reports 8 study locations across 6 states. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00606814, a Phase 1 study of Solid Tumors, has completed, sponsored by Infinity Pharmaceuticals.

COMPLETED
Registry status
Phase 1
Development phase
60 participants
Enrollment target
8
Study locations

Study Summary

This study is a Phase I clinical trial of IPI-504 in combination with docetaxel (Taxotere).The purposes of the study are to determine: * the safety profile, * the highest dose of IPI-504 that can be given with docetaxel without causing severe side effects, and * to recommend a Phase II dose of the combination in patients with solid tumors.

Conditions Studied

Interventions

  • DRUG IPI-504, docetaxel

Study Locations (8)

New York

  • Roswell Park Cancer Institute - Buffalo
  • Memorial Sloan-Kettering Cancer Center - New York

Ohio

  • Gabrail Cancer Center - Canton
  • Gabrail Cancer Center - Dover

Arizona

  • TGen Clinical Research in Scottsdale - Scottsdale

Connecticut

  • Yale Cancer Center - New Haven

Florida

  • H. Lee Moffitt Cancer Center & Research Institute - Tampa

Pennsylvania

  • University of Pittsburgh Medical Center - Pittsburgh

Trial Details

FieldValue
Enrollment Target 60 participants
Start Date 2007-12
Est. Completion 2011-12
Phase Phase 1
Infinity Pharmaceuticals

17 total trials

What the finished NCT00606814 record still lists

NCT00606814 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 60 participants, a relatively small participant target, below the 284-participant average among 125 other Solid Tumors trials with a reported enrollment target (79% lower).

The record links to 1 condition, with Solid Tumors appearing as the primary indexed condition, and to 1 intervention - of which IPI-504, docetaxel is the first listed.

NCT00606814 lists 8 locations in 6 states (New York, Ohio, Arizona).

Frequently Asked Questions

What is clinical trial NCT00606814 about?

NCT00606814 is a clinical study titled "Phase I Study of IPI-504 and Docetaxel in Patients With Advanced Solid Tumors". This study is a Phase I clinical trial of IPI-504 in combination with docetaxel (Taxotere).The purposes of the study are to determine: * the safety profile, * the highest dose of IPI-504 that can be given with docetaxel without causing severe side effects, and * to recommend a Phase II dose of the ...

What is the current status of trial NCT00606814?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 60 participants. The study started on 2007-12. Estimated completion is 2011-12.

What conditions does trial NCT00606814 study?

This clinical trial studies the following conditions: Solid Tumors.

What interventions are being tested in trial NCT00606814?

The interventions under investigation include: IPI-504, docetaxel (DRUG).

Who is sponsoring clinical trial NCT00606814?

This trial is sponsored by Infinity Pharmaceuticals, which has 17 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00606814 being conducted?

This trial has 8 study locations across Arizona, Connecticut, Florida, New York, Ohio. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Solid Tumors

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT00606814's enrollment target sits among peer trials

60 74th of 125 higher than 51 of 125 other Solid Tumors trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Solid Tumors 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

  • NCT00576069 · 60 participants

    Mechanism(s)of Airflow Limitation in Moderate-severe Persistent Asthma

  • NCT01297400 · 60 participants · Phase 2

    Phase 2 Pilot Study of the Safety and Efficacy of Topical MW-III in Thermal Burns

  • NCT01734122 · 60 participants

    Stereotactic Radiosurgery for Essential Tremor and Parkinsonian Tremor

  • NCT01804634 · 60 participants · Phase 2

    Reduced Intensity Haploidentical BMT for High Risk Solid Tumors

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 NCT00606814, the US trial registry maintained by the National Library of Medicine. NCT00606814 (small enrollment · multi site footprint · completed) retrieved and formatted by PlainTrial, see methodology.