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CRISPR Gene Therapy
CRISPR Gene Therapy is a revolutionary approach to treating genetic disorders and certain types of cancer by directly editing the DNA within a patient’s cells. 
CRISPR Gene Therapy
CRISPR Gene Therapy is a revolutionary approach to treating genetic disorders and certain types of cancer by directly editing the DNA within a patient’s cells. 

CRISPR Gene Therapy

CRISPR Gene Therapy is a revolutionary approach to treating genetic disorders and certain types of cancer by directly editing the DNA within a patient’s cells. 

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Our personalized treatment plans evolve with your cancer journey, ensuring that as your needs change, so does the level of care and support we provide. We are committed to empowering you to focus on your recovery, with treatment plans that adapt to meet your unique needs.

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How does CRISPR Gene Therapy work?

  1. Identification: The specific gene mutation or genetic sequence to be edited is identified.
  2. CRISPR-Cas9 Complex Formation: A guide RNA is designed to match the target DNA sequence, and this guide is combined with the Cas9 protein, which acts as molecular scissors.
  3. DNA Editing: The CRISPR-Cas9 complex is introduced into the patient’s cells, where it locates the target DNA sequence and makes a precise cut.
  4. Repair and Modification: The cell’s natural repair mechanisms are used to either disable the faulty gene, replace it with a healthy version, or make other desired modifications.

Target Cancers

CRISPR Gene Therapy is being explored for a wide range of conditions, including:

  1. Genetic Disorders: Such as sickle cell anemia, cystic fibrosis, and muscular dystrophy.
  2. Cancers: Including certain types of leukemia and lymphoma.
  3. Infectious Diseases: Research is ongoing to apply CRISPR for conditions like HIV.

Benefits

Precision : Allows for targeted modifications to specific genes.

Potential for Cure : Offers the possibility of correcting the underlying cause of genetic diseases.

Versatility: Can be applied to a wide range of genetic conditions.

Benefits

Precision Allows for targeted modifications to specific genes.

Potential for Cure:Potential for Cure: Offers the possibility of correcting the underlying diseases.

Versatility: Can be applied to a wide range of genetic conditions.

Risks and Side-Effects

  • Off-Target Effects: Unintended changes to other parts of the genome, which could potentially cause harmful effects.
  • Immune Reactions: The body’s immune system might react to the CRISPR components.
  • Ethical Concerns: The potential for misuse in human germline editing raises significant ethical questions.

How is it different from other Gene Therapies?

CRISPR Gene Therapy differs in several key ways:

  • Mechanism of Action: Unlike traditional gene therapy, which adds a new gene to replace a faulty one, CRISPR directly edits the existing DNA.
  • Precision: CRISPR allows for highly specific targeting of genetic sequences.
  • Potential for Wide Application: CRISPR’s versatility means it can be used for a broader range of conditions.

Eligibility Factors

Eligibility depends on factors such as:

  • Type and Severity of the Condition: The specific genetic disorder or cancer being targeted.
  • Patient’s Overall Health: General health and medical history are considered
  • Regulatory Approval: Availability of CRISPR therapy may be limited to clinical trials or specific cases, depending on regulatory approval in the region.

A thorough evaluation by a healthcare team is essential to determine if Gamma delta T – cell therapy is a suitable option.

Success Rate

Success rates vary depending on the condition being treated and the individual patient. While early results in clinical trials have shown promise, ongoing research is crucial to better understand the long-term efficacy and safety of CRISPR Gene Therapy.

During Therapy

The procedure typically involves minimal discomfort, but close monitoring is required to manage any potential side effects.

After Therapy

Follow-up visits are necessary to monitor the therapy’s effectiveness and check for any delayed side effects.

Recovery

Patients may experience mild symptoms like fatigue, but these are usually manageable.

Process

Insurance Coverage

Insurance coverage for CRISPR Gene Therapy varies by provider and plan. It is important to consult with both your healthcare provider and insurance company to understand the costs and coverage options.

Next steps if CRISPR Gene Therapy doesn’t work

Alternative options may include:

  • Alternative Gene Therapies: Other gene editing technologies or gene replacement therapies.
  • Standard Treatments: Such as chemotherapy, radiation, or surgery, depending on the condition.
  • Supportive care to manage symptoms and improve quality of life.

Contact Us

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Contact Information

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  • contact@sunactcancer.com
  • SunAct Cancer Institute Pvt. Ltd. 4th floor,
Tieten Medicity Hospital,
Kasarvadavali, Ghodbunder Road,
Thane (West) - 400615. Maharashtra, India
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  • Phone
    +9186553 13412
  • Toll free
    18002022232

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