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Phase I Study of Cisplatin Plus OSI-7904L in Patients With Solid Tumors

O

OSI Pharmaceuticals

Status and phase

Completed
Phase 1

Conditions

Advanced Solid Tumors

Treatments

Drug: OSI-7904L
Drug: Cisplatin

Study type

Interventional

Funder types

Industry

Identifiers

NCT00116896
OSI-904-102

Details and patient eligibility

About

This is a Phase I, open-label, dose escalation, study of the combination of cisplatin and OSI-7904L given on Day 1 every 21 days in patient who have advanced solid tumors.

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 18 years of age or older
  • Advanced and/or metastatic solid tumor for which no effective therapy is available
  • ECOG performance status 0-2
  • Adequate bone marrow, hepatic and renal function

Exclusion criteria

  • Patients with active or uncontrolled infections
  • Neurotoxicity >= Grade 2
  • Symptomatic brain metastases which are not stable

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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