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Clinical Trials/NCT03489525
NCT03489525
Completed
Phase 1

A Phase 1, Open-label Study to Evaluate the Safety, Pharmacokinetics, Immunogenicity, and Preliminary Efficacy of MEDI2228 in Subjects With Relapsed/Refractory Multiple Myeloma

MedImmune LLC1 site in 1 country107 target enrollmentMay 8, 2018

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Relapsed/Refractory Multiple Myeloma
Sponsor
MedImmune LLC
Enrollment
107
Locations
1
Primary Endpoint
Occurrence of SAE (serious adverse events)
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

The purpose of this study is to assess the safety, pharmacokinetics and tolerability, describe the dose-limiting toxicities (DLTs), and determine the maximum tolerated dose (MTD) or maximum administered dose (MAD [in the absence of establishing the MTD]) for single agent MEDI2228 in adult subjects with multiple myeloma who are either transplant ineligible or post autologous stem cell transplant and are relapsed/refractory.

Registry
clinicaltrials.gov
Start Date
May 8, 2018
End Date
March 21, 2022
Last Updated
4 years ago
Study Type
Interventional
Study Design
Sequential
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Subjects must be ≥ 18 years of age at the time of screening.
  • Subjects must have a confirmed diagnosis of relapsed/refractory MM as per IMWG criteria (Rajkumar et al, 2014) and have exhausted standard of care regimens with proven clinical benefit, which include agents from the following anti myeloma therapies: PIs, IMIDs, and mAbs and have measurable disease with at least one of the following criteria:
  • Serum M-protein ≥ 0.5 g/dL
  • Urine M-protein ≥ 200 mg/24 hours
  • Serum free light chain (FLC) assay: involved FLC level ≥ 10 mg/dL provided serum FLC ratio is abnormal.
  • Subjects must either be ineligible for or post-autologous stem cell transplant.
  • Eastern Cooperative Oncology Group (ECOG) performance status of 0 to
  • Adequate organ and marrow functions as determined per protocol-defined criteria.
  • Exclusion Criteria
  • Any of the following would exclude the subject from participation in the study:

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Occurrence of SAE (serious adverse events)

Time Frame: From time of informed consent through 90 days post end of treatment

To assess the occurrence of serious adverse events (SAEs)

Number of patients with changes in vital signs from baseline

Time Frame: From time of informed consent and up to 21 days post end of treatment

To assess body temperature, blood pressure and heart rate

Number of patients with changes in elctrocardiogram (ECG) results from baseline

Time Frame: From time of informed consent and up to 21 days post end of treatment

To assess using 12 lead ECG recordings

Occurrence of DLTs (dose limiting toxicities)

Time Frame: From time of informed consent through 90 days post end of treatment

To assess by the occurrence of hematologic and non-hematologic toxicities, AEs, and abnormal laboratory results

Occurrence of adverse events (AEs)

Time Frame: From time of informed consent through 90 days post end of treatment

To assess by the occurrence of adverse events (AEs)

Number of patients with changes in laboratory parameters from baseline

Time Frame: From time of informed consent and up to 21 days post end of treatment

To assess serum chemistry, hematology, coagulation and urninalysis

Secondary Outcomes

  • Duration of response (DoR)(From time of informed consent and up to three years after final patient is enrolled)
  • MEDI2228 terminal half-life for PK(From time of informed consent through 60 days post end of treatment)
  • Number of subjects who develop anti-drug antibodies (ADAs)(From time of informed consents through 60 days post end of treatment)
  • Clinical benefit rate(From time of informed consent up to three years after final patient is enrolled)
  • Progression free survival (PFS)(From time of informed consent and up to three years after final patient is enrolled)
  • MEDI2228 maximum observed concentration for PK(From time of informed consent through 60 days post end of treatment)
  • MEDI2228 area under the concentration-time curve for PK(From time of informed consent through 60 days post end of treatment)
  • MEDI2228 clearance for PK(From time of informed consent through 60 days post end of treatment)
  • Objective response rate (ORR)(From time of informed consent and up to three years after final patient is enrolled)
  • Overall Survival (OS)(From time of informed consent and up to three years after final patient is enrolled)

Study Sites (1)

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