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

NCT00704821 · ClinicalTrials.gov registry record · Phase 1

PTC299 for Treatment of Advanced Cancer

A Phase 1 study, sponsored by PTC Therapeutics.

Terminated
Registry status
Phase 1
Development phase
76
Enrollment target

NCT00704821: Clinical Trial Phase 1 study, sponsored by PTC Therapeutics.

NCT00704821 is a Phase 1 study that was terminated before completion, run by PTC Therapeutics. The registered enrollment target is 76 participants, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (27% higher). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00704821, a Phase 1 study, was terminated before completion, sponsored by PTC Therapeutics.

TERMINATED
Registry status
Phase 1
Development phase
76 participants
Enrollment target

Study Summary

Formation of new blood vessels (angiogenesis) is important for tumor growth in advanced cancer. It is known that tumors make a protein called vascular endothelial growth factor (VEGF). VEGF stimulates the formation of blood vessels that supply the tumor with nutrients and oxygen. PTC299 is an oral investigational new drug that has been shown to decrease production of VEGF in animal models of human cancer. In these animal models, oral PTC299 administration decreases VEGF levels in the tumor and in the bloodstream, decreases blood vessel numbers in the tumor, and significantly slows or halts tumor growth. When given in combination with the chemotherapeutic drug, docetaxel, PTC299 increases the antitumor activity over use of docetaxel alone. Safety studies in research animals indicate good tolerability at doses and drug levels that are higher than those planned for the clinical studies. Results from Phase 1a studies in healthy volunteers indicate that PTC299 achieves levels of PTC299 in the bloodstream that are known to be active in animal models of human cancer. This Phase 1b study is designed to test the hypothesis that PTC299 will be tolerable and will show evidence of anti-VEGF and antitumor activity when administered orally to participants with cancer.

Primary Outcome

To analyze the MTD of PTC299 within the tested dose range for use in further clinical trials in participants with advanced cancer.

Interventions

  • DRUG Docetaxel
  • DRUG PTC299

Trial Details

FieldValue
Enrollment Target 76 participants
Start Date 2008-07-03
Est. Completion 2012-02-24
Phase Phase 1
PTC Therapeutics

52 total trials

Why NCT00704821 stopped before completion

NCT00704821 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 76 participants, a relatively small participant target, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (27% higher).

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

NCT00704821 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00704821 about?

NCT00704821 is a clinical study titled "PTC299 for Treatment of Advanced Cancer". Formation of new blood vessels (angiogenesis) is important for tumor growth in advanced cancer. It is known that tumors make a protein called vascular endothelial growth factor (VEGF). VEGF stimulates the formation of blood vessels that supply the tumor with nutrients and oxygen. PTC299 is an oral i...

What is the current status of trial NCT00704821?

This trial is currently terminated. It is a Phase 1 study. The enrollment target is 76 participants. The study started on 2008-07-03. Estimated completion is 2012-02-24.

What interventions are being tested in trial NCT00704821?

The interventions under investigation include: Docetaxel (DRUG), PTC299 (DRUG).

Who is sponsoring clinical trial NCT00704821?

This trial is sponsored by PTC Therapeutics, which has 52 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00704821's enrollment target sits among peer trials

76 705th of 2000 higher than 1,290 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

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

  • NCT02615184 · 76 participants · Phase 2

    A Study to Check the Safety of Dexlansoprazole and Learn If it Can Heal Erosive Esophagitis (EE) and Keep it Healed in Children 2 to 11 Years Old

  • NCT02821741 · 76 participants · NA

    Effects of External Ear Stimulation on Pain Perception and Mood

  • NCT03019757 · 76 participants

    Distinguishing Between Alzheimer's Disease, Lewy Body Dementia, and Parkinson's Disease

  • NCT03353584 · 76 participants · NA

    Effect of Virtual Reality Technology for Pain Management of Vaso-Occlusive Crisis in Patients With Sickle Cell Disease

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT00704821, the US trial registry maintained by the National Library of Medicine. NCT00704821 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.