Newsletter | July 24, 2026

07.24.26 -- Unlocking Gentler, Cost-Efficient TIL Therapy For Cold Tumors

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Webinar: Rewriting the Code: Advances and Challenges in Pediatric Gene Therapy

Pediatric gene therapy is rapidly transforming treatment for rare genetic diseases. Join Dr. Rachel Abu Taleb as she explores AAV, lentiviral, and CRISPR platforms, reviews lessons from approved therapies, and examines the scientific, regulatory, and access challenges shaping future innovation. Learn how these advances are redefining care and improving outcomes for children with rare diseases. Click here to learn more.

FOCUS ON CLINICAL TRIALS

Unlocking Gentler, Cost-Efficient TIL Therapy For Cold Tumors

CuraCell Head of Clinical Operations Torbjörn Ström discusses, in the context of CC-38 and CytoPLY-derived tumor-infiltrating lymphocytes (TILs), the utility of named-patient experience, dosing and preconditioning, and T-cell therapy capabilities in cold solid tumors.

Galvanizing Large And Small For Clinical Success

See how two academic investigators accelerated corneal regeneration and lung fibrosis therapies from preclinical research to clinical trials by leveraging scalable GMP solutions and regulatory-ready materials.

Ethical & Regulatory Considerations For Pediatric Gene Therapy

Understanding risk thresholds, consent requirements, and IRB expectations early can prevent redesign, reduce delays, and improve trial feasibility for vulnerable patient populations

CLINICAL TRIALS SOLUTIONS

Rethinking Lab Logistics, Delivering The Complex Without Compromise - MRN - Medical Research Network

FOCUS ON SUPPLY CHAIN

Integrate Cryopreservation Into The End-To-End Supply Chain

Cryopreservation should be integrated across the entire supply chain to ensure traceability, reduce risk at handoffs, and support consistent, scalable therapy development and delivery.

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