Trial purpose
Cancer treatment
Tumor type
Haematological
Age
18+
Clinical summary
Summary
Each treatment arm in this trial receives a different treatment combination depending on stage of the study and eligibility. The study includes a dose escalation phase to determine the best dose of lemzoparlimab, followed by a dose expansion phase to confirm the dose. In the dose escalation arms, participants will receive intravenous (IV) lemzoparlimab with or without dexamethasone (orally or via IV) in combination with pomalidomide (orally) or carfilzomib (via IV) or daratumumab (via subcutaneous injection) in 28-day cycles. In the Dose Expansion arms, participants will receive the same treatments as in the Dose Escalation phase, to confirm the dose.
Conditions
This trial is treating people with relapsed or refractory multiple myeloma
Eligibility
Inclusion
-
Diagnosis of relapsed/refractory (R/R) multiple myeloma (MM) with documented evidence of progression during or after the participant's last treatment regimen based on the investigator's determination of the International Myeloma Working Group (IMWG) criteria.
- Relapsed defined as previously treated myeloma that progresses and requires initiation of salvage therapy, but does not meet criteria for refractory myeloma.
- Refractory defined as disease that is nonresponsive (failure to achieve minimal response or development of progressive disease) while on primary or salvage therapy, or progresses within 60 days of last therapy.
- Measurable disease per the protocol within 28 days prior to enrollment.
-
Arm A - Lemzoparlimab with or without Dexamethasone
- For Both Escalation and Expansion Phase, participant must have refractory to 3 prior lines of treatment of anti-myeloma treatments, as outlined in the protocol.
-
Arm B - Lemzoparlimab + Pomalidomide-Dexamethasone
- For Escalation Phase - Participant must have received at least 3 prior lines of therapy, as outlined in the protocol.
- For Expansion Phase- Participant must have received at least 2 prior line of therapy, as outlined in the protocol.
-
Arm C - Lemzoparlimab + Carfilzomib-Dexamethasone
- For Escalation Phase- Participant must have received at least 3 prior lines of therapy as outlined in the protocol.
- For Expansion Phase- Participant must have received at least 1 prior line of therapy.
- Arm D - Lemzoparlimab + Daratumumab-Dexamethasone -- For Both Escalation and Expansion Phase - Participant must: --- Have received at least 3 prior lines of therapy, as outlined in the protocol.
Exclusion
-
Arm B - Lemzoparlimab + Pomalidomide-Dexamethasone
- For Both Escalation and Expansion Phase participant must have had no prior treatment with pomalidomide.
-
Arm C - Lemzoparlimab + Carfilzomib-Dexamethasone
- For Both Escalation and Expansion Phase - prior treatment with carfilzomib.
-
Arm D - Lemzoparlimab + Daratumumab-Dexamethasone
- For Both Escalation and Expansion Phase - prior treatment with daratumumab or other anti-CD38 therapy.
Inclusion
- You are able to swallow medication by mouth.
- You have had treatment but your cancer has gotten worse or has not responded to the treatment you have been given.
- You have had treatment, but your cancer has come back (relapsed or recurrent).
Exclusion
- You have had certain treatments, surgical procedures or drugs.
Clinical trials have complex eligibility criteria, and other criteria may apply for this trial. Ask your doctor about whether this trial could be right for you.
More information
Trial Identifiers
Information on this page is partially produced from ClinicalTrials.gov *. View further details about this trial on the registry via the links below:
Trial sponsor
AbbVie
Scientific Title
A Phase 1b, Dose Escalation and Expansion Study of Lemzoparlimab With or Without Dexamethasone and in Combination With Anti-Myeloma Regimens for the Treatment of Patients With Relapsed/Refractory Multiple Myeloma
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