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Completed

NCT Number: NCT00276302

Safety Study of IPI-504 in Patients With Gastrointestinal Stromal Tumors (GIST) or Soft Tissue Sarcomas (STS)

The primary objectives of the study are:

* Determine the safety and maximum tolerated dose (MTD) of IPI-504 in GIST and STS patients who have failed prior therapies * Recommend a dose for subsequent studies of IPI-504

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Mount Sinai Hospital, Toronto, Ontario, Canada

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About this study

IPI-504 is a novel, water-soluble analog of 17-AAG and a potent inhibitor of Hsp90. Hsp90's role in the cell is to control the proper folding, function, and viability of various "client" proteins. Many of these client proteins (such as AKT, Her-2, Bcr-Abl, PDGFR-α, and c-Kit) are oncoproteins or important cell signaling proteins. In patients with GIST, mutations in the tyrosine kinase receptor Kit play a critical role in the pathogenesis of this disease. Inhibition of Kit signaling with the tyrosine kinase inhibitor Imatinib (IM) is a very effective treatment for GIST patients. However, new mutations arise in Kit conferring resistance to IM treatment which results in disease progression. Kit is a client protein of Hsp90 and is sensitive to IPI-504. In Soft Tissue Sarcomas, there may be genetic abnormalities that lead to the expression of certain proteins that drive the growth of cancer. These cancer-driving proteins may be stimulated by HSP90. This provides a scientific rationale for Phase 1 clinical testing of IPI-504 in patients with advanced GIST and STS who have failed prior therapies.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Pathologically confirmed diagnosis of GIST or STS
  • Failed prior therapies
  • ECOG performance status of 0-2
  • Ability to adhere to the study visit schedule and all protocol requirements

Exclusion criteria

  • Previous treatment with 17-AAG, DMAG, or other known Hsp90 inhibitor
  • Participation in any investigational drug study or treatment with any other kinase inhibitor therapy within 2 weeks preceding start of treatment
  • Concurrent radiation therapy is not permitted
  • Concurrent treatment with any agent that alters CYP3A activity
  • Concurrent treatment with any agent that may prolong the QTc interval
  • Myocardial infarction or active ischemic heart disease within 6 months
  • History of arrhythmia
  • Baseline QTc >450
  • Grade 3 or greater peripheral neuropathy
  • Renal insufficiency, serum creatinine >1.5 x ULN
  • Platelets < 100,000 mm3
  • AST and / or ALT > 2.5 x ULN
  • ANC <1,500 cells/mm3
  • Alkaline phosphatase > 2.5 x ULN
  • Amylase and lipase > 1.5 x ULN
  • Hemoglobin < 9.0 g/dL

Treatment and study plan

IPI-504

Drug

IV administration of IPI-504 for 21-day cycles. Two different schedules of treatment will be tested. On Schedule A, doses occur on Days 1, 4, 8, and 11 followed by 10 days with no study drug administration. On Schedule B, doses occur on Days 1, 4, 8, 11, 15, and 18, or twice weekly for 3 weeks continuously.

For both Schedule A and B doses will be administered ≥ 72 hours apart.

Primary outcomes

  1. To determine the safety and maximum tolerated dose (MTD) of IPI-504 in GIST and STS patients who have failed prior therapies

    Time frame: 18 months

  2. To recommend a dose for subsequent studies of IPI-504

    Time frame: 18 months

Secondary outcomes

  1. To examine the pharmacokinetic (PK) parameters of IPI-504 in GIST and STS patients

    Time frame: 18 months

  2. To assess in a preliminary way the potential anti-tumor activity of IPI-504 in GIST and STS.

    Time frame: 18 months

  3. To explore potential pharmacodynamic (PD) markers of biologic activity of IPI-504 in GIST and STS.

    Time frame: 18 months

Sponsors and collaborators

Lead sponsor

Infinity Pharmaceuticals, Inc.

Industry

Registry information

Official study title

A Phase 1, Safety Assessment and Pharmacokinetic Study of IPI-504 in Patients With Either Metastatic and/or Unresectable Gastrointestinal Stromal Tumors (GIST) or Advanced or Metastatic Soft Tissue Sarcomas (STS)

Important dates

Study start
2005
Primary completion
2010
Study completion
2010
First posted
Jan 13, 2006
Registry last updated
Jan 6, 2011

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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