Summary

Eligibility
for people ages 18 years and up (full criteria)
Location
at Orange, California and other locations
Dates
study started

Description

Summary

Elranatamab is a bispecific antibody: binding of elranatamab to CD3- expressing T-cell and BCMA- expressing multiple myeloma cells causes targeted T-cell mediated cytotoxicity. This expanded access protocol will provide access to elranatamab until it becomes commercially available to patients who are refractory to at least one proteasome inhibitor, one immunomodulatory drug and one anti-CD38 antibody and have no access to other comparable/alternative therapy and for whom elranatamab could be a possible treatment option.

Official Title

ELRANATAMAB (PF-06863135) MONOTHERAPY EXPANDED ACCESS PROTOCOL FOR TREATMENT OF PATIENTS WITH RELAPSED/REFRACTORY MULTIPLE MYELOMA WHO ARE REFRACTORY TO AT LEAST ONE PROTEASOME INHIBITOR, ONE IMMUNOMODULATORY DRUG AND ONE ANTI-CD38 ANTIBODY AND HAVE NO ACCESS TO OTHER COMPARABLE/ALTERNATIVE THERAPY

Details

Study C1071017 is a single-arm, open-label study in patient with relapsed /refractory multiple myeloma. Each patient will receive study intervention until disease progression, unacceptable toxicity, withdrawal of consent, study termination or until elranatamab becomes commercially available.

Keywords

Multiple Myeloma, Erlanatamab, Expanded Access, Plasma Cell Neoplasms, Elranatamab (PF-06863135)

Eligibility

You can join if…

Open to people ages 18 years and up

  • Prior diagnosis of MM as defined according to IMWG criteria .
  • Patients who are ineligible for participation in any ongoing clinical trial of elranatamab, including lack of access due to geographical limitations, and who have exhausted all other treatment options.
  • Measurable disease based on IMWG criteria as defined by at least 1 of the following:
  • Serum M-protein ≥0.5 g/dL (≥5 g/L)
  • Urinary M-protein excretion ≥200 mg/24 hours
  • Involved FLC ≥10 mg/dL (≥100 mg/L) AND abnormal serum immunoglobulin kappa to lambda FLC ratio (<0.26 or >1.65).
  • Refractory to at least one IMiD, one PI, and one anti-CD38 antibody.
  • Relapsed/refractory to last anti-MM regimen.
  • ECOG performance status 0-1.
  • Resolved acute effects of any prior therapy to baseline severity or CTCAE Grade ≤1.
  • Not pregnant, willing to use contraception

You CAN'T join if...

  • Smoldering MM; plasma cell leukemia; POEMS syndrome; Waldenström's macroglobulinemia; amyloidosis; stem cell transplant within 12 weeks prior to enrollment or active GVHD
  • Previous treatment with BCMA directed therapy;
  • SARS-CoV2, HIV, HBV, HCV or any active, uncontrolled bacterial, fungal, or viral infection.

Active infections must be resolved at least 14 days prior to enrollment.

  • Any other active malignancy within 3 years prior to enrollment, except for adequately treated basal cell or squamous cell skin cancer, carcinoma in situ or Stage 0/1 with minimal risk of recurrence per treating physician.
  • Previous administration with an investigational drug or vaccine within 30 days (or as determined by the local requirement) or 5 half-lives preceding the first dose of study intervention used in this study (whichever is longer)

Locations

  • UC Irvine Health not accepting new patients
    Orange California 92868 United States
  • UC Irvine Medical Center not accepting new patients
    Orange California 92868 United States
  • Ronald Reagan UCLA Medical Center not accepting new patients
    Los Angeles California 90095 United States
  • UCLA Hematology/Oncology - Westwood (Building 200 Suite 120) not accepting new patients
    Los Angeles California 90095 United States

Details

Status
not accepting new patients
Start Date
Sponsor
Pfizer
Links
To obtain contact information for a study center near you, click here.
ID
NCT05462639
Study Type
Expanded Access
Last Updated