Multiple Myeloma Clinical Trials

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Pilot, Open-Label, Single-Arm Study of Autologous BCMA-Directed CAR-T Cells in Patients With Relapsed/Refractory Multiple Myeloma in Pakistan

Status: Recruiting
Location: See all (2) locations...
Intervention Type: Biological
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

The treatment options for multiple myeloma have evolved significantly over the years, providing patients with a range of therapies tailored to their specific circumstances. The choice of treatment often hinges on various factors, including the aggressiveness of the disease, individual prognostic indicators like genetic markers, the overall physical condition of the patient, and any pre-existing health issues that may affect treatment decisions. Current therapeutic strategies include several classes of drugs, each working through different mechanisms. Proteasome inhibitors (PIs) disrupt the protein degradation process within myeloma cells, thereby promoting their death. Immunomodulatory drugs (IMiDs) modulate the immune system and inhibit tumor growth by enhancing the body's natural anti-cancer responses. Monoclonal antibodies specifically target cancer cells, marking them for destruction by the immune system. In cases where patients are eligible, autologous stem cell transplantation remains a viable option, offering the potential for long-term remission by replacing damaged bone marrow with healthy stem cells from the patient's own body. Despite these advancements, multiple myeloma continues to present significant challenges, as it often recurs even after initial successful treatment and remains an incurable disease. This highlights the urgent need for innovative therapeutic strategies that can effectively address resistance to existing treatments, ultimately aiming to improve patient outcomes and survival rates.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Male and female participants of age 18 years and above.

• Patients with a confirmed diagnosis of multiple myeloma according to IMWG diagnostic criteria.

• Received at least 3 prior multiple myeloma treatment lines of therapy or are double refractory to an IMiD and PI (refractory multiple myeloma as defined by IMWG consensus criteria). Note: induction with or without hematopoietic stem cell transplant and with or without maintenance therapy is considered a single line of therapy.

• Measurable disease at Screening as per IMWG criteria.

• ECOG Performance Status grade of 0 to 2.

• Adequate organ function: ANC/platelets thresholds (unless cytopenias attributable to MM), LVEF ≥45%, adequate oxygenation; hepatic/renal criteria specified in Section 10.

• Negative pregnancy test for women of childbearing potential; agreement to effective contraception.

• Patients giving written informed consent to participate in the study after a full understanding of the implications and constraints of the study protocol.

• Understand the content of the ICF, and voluntarily sign the ICF (If the participant is unable to sign the ICF on their own due to illiteracy, an impartial witness is needed).

⁃ The subject can understand the research process and is willing and able to comply with all research proposals and other requirements of the study.

⁃ Willing and able to adhere to the prohibitions and restrictions specified in this protocol.

Locations
Other Locations
Pakistan
National University of Medical Sciences, Clinical Trial Unit
RECRUITING
Rawalpindi
National University of Medical Sciences, Clinical Trial Unit
RECRUITING
Rawalpindi
Contact Information
Primary
Nadia Sial, Ph.D
nadiaharif@gmail.com
+923315582265
Backup
Maryam Khan, MBBS, MRCP(UK), FCPS (Cl Haem)
+923366395758
Time Frame
Start Date: 2026-06-01
Estimated Completion Date: 2027-12-31
Participants
Target number of participants: 10
Treatments
Other: CAR-T arm
6.2. Screening Phase During the Screening period, all participants will be asked to provide written consent for study participation and will be screened for study eligibility within 28 days before apheresis. Safety criteria that must be met before starting apheresis are presented in Section 8.1.1.~If an assessment was performed as part of the participant's routine clinical evaluation and not specifically for this study, it does not need to be repeated after signed informed consent has been obtained, provided the assessments fulfill the study requirements and are performed within the specified timeframe before the first dose of study treatment. Retesting of abnormal screening values that lead to exclusion is allowed only once during the screening phase (to reassess eligibility). The last result obtained before apheresis will be used to determine eligibility. Subjects who do not meet all inclusion criteria or who meet an exclusion criterion may, at the discretion of the investigator,
Related Therapeutic Areas
Sponsors
Leads: Dr. Zaineb Akram

This content was sourced from clinicaltrials.gov