Next-Generation
Cellular
Immunotherapy

Personalized, targeted treatment approaches that harness the body's own immune cells to fight cancer.

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CELLULAR IMMUNOTHERAPY

What Is Cell Therapy?

Cell therapy is a next-generation treatment approach that uses the patient's own immune cells or donor-derived cells to combat disease, particularly cancer. Unlike conventional chemotherapy and radiation, it destroys only target cells without harming healthy tissue.

2024 6 FDA-approved cell therapy products on the market

The CAR-T era began in 2017 with the FDA approval of Kymriah. By early 2024, it had grown to six products: Kymriah, Yescarta, Tecartus, Breyanzi, Abecma, and Carvykti.

These therapies are used in the following cancers:

• Childhood leukemia (B-ALL)
• Large B-cell lymphoma
• Mantle cell lymphoma
• Multiple myeloma (bone marrow cancer)

By late 2024, two new approvals reached solid tumors as well: AMTAGVI (for melanoma) and TECELRA (for synovial sarcoma).

Bottom line: Cell therapy is no longer experimental. It has become a regulatory-approved, evidence-based treatment standard.

80%+ Overall response rate in hematologic cancers

CAR-T cell therapy response rates vary by cancer type. Results from two pivotal trials:

Pediatric leukemia (B-ALL): 81% complete remission in the ELIANA trial (Maude et al., NEJM 2018)
Refractory large B-cell lymphoma: 83% overall response and 58% complete response in the ZUMA-1 trial (Neelapu et al., NEJM 2017)
5-year follow-up: 42.6% of patients still alive

Bottom line: These rates show that in refractory cases where conventional chemotherapy and radiation have failed, cell therapy is a life-saving option.

$14B+ 2025 global cell therapy market size

The global cell therapy market is growing rapidly:

2025 valuation: $7-18 billion (varies by research firm)
2034 projection: expected to exceed $47 billion
Annual growth: above 20%

Three forces drive this growth: expansion of CAR-T therapies into new cancer types, declining manufacturing costs, and increasing patient access in emerging markets.

Bottom line: With cGMP-compliant domestic manufacturing in Türkiye, Genkord Therapeutics holds a strategic position in this rapidly growing global market.

TREATMENT PLATFORMS

Genkord's Ministry-Approved Therapy Platforms

Genkord Therapeutics manufactures three ministry-approved cellular therapy platforms in its own cGMP-certified laboratory.

APPROVED
NK Cell

NK Cell

Natural Killer Cell

The elite warriors of innate immunity. Capable of recognizing and destroying tumor cells instantly without prior sensitization. A safe treatment option with a favorable side-effect profile.

Innate Recognition Low Toxicity Allogeneic Use
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APPROVED
CIK Cell

CIK

Cytokine-Induced Killer Cell

Cytokine-activated killer cells combining NK and T cell properties. Their hybrid phenotype enables broad-spectrum anti-tumor activity with MHC-unrestricted target recognition.

Hybrid Phenotype Broad Spectrum Ex Vivo Production
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APPROVED
Dendritic Cell

DC

Dendritic Cell

The "teacher" cells of the immune system. They process and present tumor antigens to T cells, triggering a potent, targeted immune response. The foundation of personalized cancer vaccine approaches.

Antigen Presentation Immune Priming Cancer Vaccine
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ADVANTAGES

Why Cell Therapy?

Conventional Approaches

  • Cannot distinguish between healthy and cancerous cells
  • Systemic side effects (nausea, hair loss, immunosuppression)
  • Resistance development with repeated treatment
  • No lasting immunological memory after treatment
VS

Cellular Immunotherapy

  • Selectively targets only cancer cells
  • Fewer side effects, higher quality of life
  • Alternative mechanisms against resistant tumors
  • Long-term protection through immunological memory

Domestic Manufacturing
Power in Cell Therapy.

Operating in cell biology since 2003, Genkord develops and manufactures ministry-approved cellular immunotherapy products in its own cGMP-certified R&D facility.

Integrated Manufacturing

All processes from cell isolation to final product are carried out under one roof in our cGMP-certified R&D facility.

Deep R&D Heritage

Over 20 years of cell biology expertise. More than 15 biological products successfully developed and commercialized.

Approved Therapy Portfolio

NK cell, CIK, and Dendritic Cell: three distinct ministry-approved cellular therapy platforms actively in production.

2003 Founded
15+ Biological Products
cGMP Certified Manufacturing
3 Approved Therapy Platforms

Interested in Learning More
About Cell Therapy?

Get in touch with our team for R&D collaborations, clinical study partnerships, or product information.