QLS4131
DrugQLS4131 will be administered subcutaneously.
NCT Number: NCT07560449
The purpose of the study is to compare the efficacy of QLS4131(SC) in combination with QL2109, with or without pomalidomide or lenalidomide, and QLS4131 (SC) in combination with QL2109, and QLS4131 (SC) in combination with Pomalidomide, and QLS4131(SC) in combination with QL2109 and Lenalidomide.
Trial opening soon.
Get Notified18 year and older
All sexes
Interventional
Phase 2
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
For patients with multiple myeloma and plasma cell leukemia, measurable disease at screening is defined as meeting any one of the following:
For patients with light-chain amyloidosis:Measurable disease is defined as Involved serum free light chain ≥ 50 mg/L with an abnormal light chain ratio,ordifference between involved and uninvolved serum free light chains (dFLC) ≥ 50 mg/L.
Exclusion criteria
QLS4131 will be administered subcutaneously.
QL2109 will be administered subcutaneously.
Pomalidomide will be self-administered as a single dose orally.
Lenalidomide will be self-administered as a single dose orally.
Dexamethasone will be administered orally or intravenously.
Time frame: From time of the first dose of QLS4131 to end of DLT period (28 days)
To evaluate the tolerability and safety of subcutaneous administration of QLS4131 for Injection in combination with other agents in patients with malignant plasma cell neoplasms
Time frame: Up to 2 years
To determine the maximum tolerated dose (MTD)
Time frame: Up to 2 years
Overall response (PR or better) is defined as percentage of participants who have a PR or better per International Myeloma Working Group (IMWG) criteria.
Time frame: Up to 2 years
MRD-negative is defined as proportion of participants who achieve MRD negativity at a threshold of 10^-5 at any timepoint after the first dose of study drug and before disease progression or start of subsequent antimyeloma therapy.
Contact information is provided by the study sponsor or research team.
Qilu Pharmaceutical Co., Ltd.
Industry
A Multicenter, Open-Label Phase II Study to Evaluate QLS4131 Combination Therapy in the Treatment of Malignant Plasma Cell Neoplasms
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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.