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Expanded Access Use of L-MTP-PE for the Treatment of Osteosarcoma

Memorial Sloan Kettering Cancer Center (MSK) logo

Memorial Sloan Kettering Cancer Center (MSK)

Status

Conditions

Osteosarcoma

Treatments

Drug: L-MTP-PE

Study type

Expanded Access

Funder types

Other

Identifiers

Details and patient eligibility

About

This expanded access protocol will allow access to treatment with L-MTP-PE for people with osteosarcoma. L-MTP-PE is an investigational drug that has not been approved by the FDA to treat any condition, including osteosarcoma. L-MTP-PE works by activating certain types of white blood cells, and these active white blood cells help the immune system kill cancer cells.

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Confirmed diagnosis of osteosarcoma of any age Note: Patients with either newly diagnosed or relapsed osteosarcoma are eligible.

  • Surgical resection or other definitive local control therapy of all clinically detectable sites of osteosarcoma

  • L-MTP-PE is deemed to be of potential benefit by the treating investigator

  • Willing and able to understand and sign informed consent and assent as appropriate

  • Life expectancy > 6 weeks

  • Adequate organ function as follows:

  • Adequate bone marrow function defined as:

    • absolute neutrophil count (ANC) ≥ 750/mm^3
    • platelet count ≥ 30,000/ mm^3
    • hemoglobin ≥ 8 g/dl
  • Adequate renal function defined as:

    • Creatinine clearance or radioisotope glomerular filtration rate ≥ 70 mL/min/1.73m^2 OR
    • Serum creatinine ≤ 2x the upper limit of normal based on age/gender
  • Adequate liver function defined as:

    • Bilirubin (sum of conjugated + unconjugated) ≤ 2x upper limit of normal for age or ≤ 4x upper limit of normal if thought to have Gilbert's disease
    • AST or ALT ≤ 3x upper limit of normal or ≤ 5x upper limit of normal for patients with liver metastases
  • Willing to use a barrier method of contraception throughout the course of the study and for 1 year after participation if relevant

Exclusion criteria

  • Use of chronic steroids of other immunosuppressive agents
  • Pregnant or breast feeding

Trial contacts and locations

1

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Central trial contact

Emily Slotkin, MD; Paul Meyers, MD

Data sourced from clinicaltrials.gov

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