Cartilage Regeneration Therapy

Don't let knee pain define your life

Cartilage defects generally do not heal on their own. RECARTA is an autologous chondrocyte therapy that uses the patient’s own cartilage cells.

RECARTA is an autologous chondrocyte therapy manufactured by KELI Therapeutics in a licensed GMP facility in Kaunas, Lithuania. The treatment is performed in two surgical stages: cartilage biopsy, then cell culture and manufacture, followed by implantation.

RECARTA | Autologous Chondrocyte Therapy
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Active person enjoying life after cartilage treatment
RECARTA
Autologous Chondrocyte Therapy

RECARTA | Autologous Chondrocyte Therapy

Person sitting on a park bench holding their knee after a cartilage injury
Understanding the Problem

Cartilage damage doesn't heal on its own

Articular cartilage is the smooth, protective tissue covering the ends of bones in your joints. Unlike other tissues in your body, cartilage has no blood supply and very limited ability to repair itself.

When cartilage is damaged — whether from injury, sports, or wear — the defect tends to worsen over time, leading to pain, swelling, and reduced mobility. Without proper treatment, this can progress to osteoarthritis.

RECARTA Solution

Your own cells, regenerating your cartilage

RECARTA is autologous chondrocyte therapy (ACT). It uses your own cartilage cells, cultivated and implanted to regenerate healthy tissue.

Autologous chondrocyte therapy

RECARTA uses the patient’s own cartilage cells.

Licensed GMP manufacture

KELI Therapeutics manufactures RECARTA in a licensed GMP facility in Kaunas, Lithuania.

Individual treatment planning

Suitability, surgery, and rehabilitation are planned with the treating orthopaedic surgeon.

Published clinical research

The evidence base draws on published research in autologous chondrocyte implantation, including matrix-associated techniques.

Microscopy image of cultured chondrocytes — the cartilage cells used in RECARTA therapy
Phase-contrast microscopy · Cultured chondrocytes
The Building Blocks

Meet the chondrocytes

What you see in this image are chondrocytes — the specialized cells responsible for producing and maintaining cartilage tissue. These are the very cells that RECARTA uses to regenerate your damaged knee cartilage.

In RECARTA process, a small sample of your own chondrocytes is harvested during a minimally invasive biopsy. They are then carefully multiplied in our licensed facility over approximately four weeks, producing millions of healthy, patient-specific cells.

Once cultivated, these cells are applied to a biocompatible membrane and implanted into the cartilage defect — where they integrate with surrounding tissue and produce new, hyaline-like cartilage that closely resembles the original.

Treatment Process

The RECARTA treatment process

The treatment involves two surgical stages, with a controlled laboratory manufacturing phase in between.

01

Stage 1: Cartilage biopsy

The surgeon collects a small cartilage biopsy to prepare the individual treatment.

First surgical procedure
02

Laboratory phase: cell culture and manufacture

The cartilage cells are isolated from the biopsy sample and cultured under controlled conditions in KELI Therapeutics’ licensed GMP facility in Kaunas, Lithuania.

Licensed GMP facility
03

Stage 2: Implantation

The prepared RECARTA product is implanted into the cartilage defect.

Second surgical procedure
04

Rehabilitation

The rehabilitation plan is agreed individually with the treating specialist.

Individual plan

Could RECARTA be right for you?

Take our quick eligibility assessment to find out if cartilage cell therapy could help with your knee condition. It takes less than 2 minutes and your answers will be reviewed by a medical specialist.

  • No referral needed to start
  • Free, no-obligation assessment
  • Reviewed by our medical team
  • Response timing depends on the individual review
RECARTA

Why trust RECARTA?

RECARTA rests on two things: decades of published chondrocyte therapy research, and our own manufacturing and preclinical data.

30+ years of published research

Chondrocyte therapy was first described in 1994. Third-generation membrane-based therapies have 10–20 years of follow-up data.

Licensed and audited manufacturing

KELI Therapeutics' laboratory in Kaunas is audited by VVKT against GMP requirements and holds a manufacturing permit for RECARTA.

Nationally authorised therapy

RECARTA is provided under the Hospital Exemption framework — a nationally supervised pathway for advanced therapies.

Long-term results in the literature

Published studies of third-generation chondrocyte therapies report 88–93% patient satisfaction at 10 years.

Free Patient Guide

Everything you need to know about cartilage cell therapy

Download PDF
Clinical Evidence

Published clinical research

RECARTA is supported by published clinical research in autologous chondrocyte implantation. The evidence base includes matrix-associated techniques used to treat focal knee cartilage defects.

Treatment decisions should be individual, based on the cartilage defect, joint condition, and the patient’s goals.

— discuss with an orthopaedic specialist
View all clinical evidence
>90%
Cell viability at release
KELI Therapeutics quality data
30+ years
Years of published chondrocyte research
Since Brittberg et al., NEJM 1994
88–93%
Patient satisfaction at 10 years
Published MACI studies, Ebert et al., 2024
Cost and Insurance

Understanding treatment costs

We believe cost should not be a barrier to accessing advanced cartilage therapy. Our team can help you navigate insurance coverage and financing options.

Insurance Coverage

Coverage and insurance options depend on the country and insurer.

Documentation Support

Our patient coordinators assist with insurance pre-authorization, medical necessity documentation, and appeals if needed.

Individual decision

Discuss treatment options with your doctor, taking account of clinical alternatives, rehabilitation, and possible costs.

Common Questions

Frequently asked questions

Get quick answers to the most common questions about RECARTA cartilage cell therapy.

View all FAQs

Who is a good candidate for RECARTA?

RECARTA may be considered for people with focal knee cartilage defects. A qualified orthopaedic specialist must assess the cartilage lesion, knee stability, alignment, other joint changes, and rehabilitation plan before determining suitability.

How long does recovery take?

The rehabilitation plan and timing of return to activities are agreed individually with the treating specialist.

Is RECARTA covered by insurance?

Coverage and insurance options depend on the country and insurer.

How effective is the treatment?

Published studies of third-generation chondrocyte therapies report 88–93% patient satisfaction at 10 years and lasting improvement in knee function. RECARTA is made on the same principle. Our own preclinical studies confirmed the cells' ability to form cartilage tissue, and every batch meets strict quality specifications before use. Individual results vary.

Orthopaedic surgeons discussing RECARTA treatment case
For Healthcare Professionals

Partner with KELI Therapeutics

Access detailed clinical protocols, ordering information, and scientific resources for RECARTA membrane-associated chondrocyte implantation therapy.

  • Detailed indications and contraindications
  • Step-by-step surgical protocol
  • Ordering and logistics information
  • Clinical training and support
Healthcare Professional Portal

Take the first step toward pain-free movement

Whether you're exploring options or ready to begin, our team is here to help. Start with a free eligibility assessment or speak directly with a patient coordinator.