پرش به محتوای اصلی

R&D PIPELINE & CLINICAL PROGRAMS

Advancing next-generation cellular & gene therapies

CARA Yakhteh is building a deep, scientifically diversified pipeline aimed at life-threatening hematologic malignancies and severe genetic hemoglobin disorders. By harnessing autologous cell engineering, synthetic immunology, and CRISPR-based genome editing, we translate frontier biology into clinical reality.

Explore our investigational programs below to review the disease biology, targeted molecular mechanisms, and prospective development pathways.

Iranian biotechnology researchers monitoring cell therapy R&D data in Tehran cleanroom laboratory
Candidate Portfolios

Investigational Programs in Focus

Our active research and development portfolio focused on relapsed hematologic cancer and congenital blood disorders.

CAR T cells targeting Multiple Myeloma malignant plasma cells
IN DEVELOPMENT • MM
Cellular Immunotherapy

BCMA-Targeted CAR T-Cell Therapy for Multiple Myeloma

Autologous T cells engineered to express a chimeric antigen receptor recognizing B-cell maturation antigen (BCMA), directing personalized cytotoxic responses toward malignant plasma cells.

Target: BCMA Autologous T Cells Synthetic Biology
CRISPR genome editing targeting BCL11A for hemoglobinopathies
IN R&D • HEMOGLOBINOPATHIES
Precision Genome Editing

CRISPR-Based Therapy for β-Thalassemia & Sickle Cell

Ex vivo genome editing of autologous hematopoietic stem cells targeting the BCL11A erythroid enhancer to downregulate fetal hemoglobin suppression and restore functional oxygen transport.

Target: BCL11A Enhancer CRISPR-Cas9 HbF Reactivation