Clinical Trials Directory

Trials / Terminated

TerminatedNCT00911248

PTC299 for Treatment of Neurofibromatosis Type 2

A Phase 2 Study to Assess the Efficacy, Safety, and Pharmacodynamic Activity of PTC299 in Patients With Neurofibromatosis Type 2

Status
Terminated
Phase
Phase 2
Study type
Interventional
Enrollment
11 (actual)
Sponsor
PTC Therapeutics · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Formation of new blood vessels (angiogenesis) is important for tumor growth in neurofibromatosis type 2 (NF2). It is known that tumors make a protein called vascular endothelial growth factor (VEGF) and there are higher levels of VEGF in the tumors and blood of many patients with NF2. VEGF stimulates the formation of blood vessels that supply the tumor with nutrients and oxygen. PTC299 is an oral 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. 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 tumor. This Phase 2 study is designed to test the hypothesis that PTC299 will be tolerable and will show evidence of VEGF reduction, antitumor activity, and hearing improvement when administered orally to patients with NF2.

Detailed description

The study will be conducted in 2 stages. In Stage 1 of the study, 11 patients will receive daily treatment with PTC299 administered at 100 mg/dose twice per day for up to 1 year or until tumor progression. If no subject responds with tumor shrinkage or an improvement in hearing, then the study will be stopped. If ≥1 out of 11 subjects respond, then the study will proceed to Stage 2 to enroll an additional 14 subjects for a total of 25 subjects.

Conditions

Interventions

TypeNameDescription
DRUGPTC299PTC299 will be administered orally at 100 mg/dose twice per day for up to 1 year or until tumor progression

Timeline

Start date
2009-07-31
Primary completion
2012-03-31
Completion
2012-03-31
First posted
2009-06-01
Last updated
2019-04-12

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00911248. Inclusion in this directory is not an endorsement.

PTC299 for Treatment of Neurofibromatosis Type 2 (NCT00911248) · Clinical Trials Directory