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Q-REstrain Therapy

A breakthrough in personalized, autologous therapy for cancer

Q-REstrain is a breakthrough in personalized, autologous therapy for cancer—a sophisticated non-manipulated, personalized therapy that targets the specific genetic sequences driving a patient’s cancer, viral infections, or Lyme disease and inhibits expression of those genetic sequences. This innovative personalized, autologous therapy goes beyond traditional approaches by creating a uniquely tailored treatment designed specifically for individual needs.

This therapy available to various countries (excluding Singapore).

What is Q-REstrain?

Advanced microRNA for Cancer

Autologous Therapy
Q-REstrain is completely personalized to the patient. Using a simple blood sample, our laboratory scientists analyze the patient’s specific genetic markers to create a therapy that targets only the desired genes.

Gene Silencing
Q-REstrain utilizes advanced RNA technology to "silence" problematic genetic sequences. This advanced therapy in cancer uses small oligonucleotide molecules that are complementary to specific gene sequences, effectively turning off the signals that allow certain cancers, viruses, or Lyme disease to thrive through precise gene silencing technology. By blocking specific messenger RNA (mRNA) sequences, Q-REstrain prevents proteins essential for cell survival or metabolism from being produced in your body.

How Does Q-REstrain Work?

Q-REstrain takes advantage of oligonucleotide molecules – microRNAs isolated by the patient’s sample. The Q-REstrain molecule has a potent ability to block specific mRNA with a very high rate of specificity; therefore expression of only the desired gene is inhibited.

 

5-Step Process

Certified RGCC practitioners receive training and support through RGCC college and the RGCC practitioner network.

1. Consultation

Patient connects with a trained RGCC practitioner who evaluates their case and determines if Q-REstrain is a good fit.

2. Pre-Testing

Patient completes required diagnostic tests (Oncotrace for cancer)

3. Blood Collection

Patient provides blood sample for personalized therapy development.

4. Therapy Production

Customized Q-REstrain therapy is created in our state-of-the-art laboratory (14 working days).

5. Treatment

Patient receives personalized therapy through an RGCC practitioner.

How does Q-REstrain help?

Based on antisense therapy, Q-REstrain targets the genes responsible for cancerous growths; the natural outcome is a breakdown of the cancer cells and an overall reduction of tumor volume.

It offers a highly positive response, the initial objective is to stop cancer progression, and the secondary objective is to eliminate cancer cells. Q-REstrain achieves this whilst avoiding damage to normal cells.

Who is Q-REstrain For?

Q-REstrain therapy offers hope and healing for patients facing multiple challenging conditions:

Cancer

Solid Tumors: Effective for most solid tumor types across various stages Hematologic Malignancies: Blood cancers including leukemias, lymphomas, and myelomas

Note: CNS (central nervous system) cancers are not suitable for Q-REstrain therapy

Viruses

Q-REstrain successfully targets a comprehensive range of viral infections, such as:

Herpes Viruses: HSV1/HSV2, HHV6, Varicella Zoster (shingles), Epstein-Barr Virus (EBV), Cytomegalovirus (CMV)

Human Papilloma Virus: HPV-16/18 and HPV-6/11

Hepatitis: Hepatitis B and C viruses

Other Viruses: Coxsackie Virus, HIV, HTLV1

Lyme Disease

Targeted treatment for Lyme disease and associated co-infections, helping patients overcome these complex, chronic conditions.

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Therapy Details

Is Q-REstrain Safe?

Q-REstrain therapy has been extensively studied with thousands of research studies confirming its safety profile. The therapy is well-tolerated by most patients, with a strong track record of successful outcomes across diverse patient populations.  

Sample of Studies:  

Safety of antisense oligonucleotide and siRNA-based therapeutics

https://www.sciencedirect.com/science/article/abs/pii/S1359644617300430

Antisense oligonucleotides as therapeutic agents

https://doi.org/10.1002/(SICI)1097-4652(199911)181:2%3C251::AID-JCP7%3E3.0.CO;2-D

In vivo and in vitro studies of antisense oligonucleotides – a review

https://pubs.rsc.org/en/content/articlehtml/2020/ra/d0ra04978f

Therapeutic Antisense Oligonucleotides Are Coming of Age

https://www.annualreviews.org/doi/abs/10.1146/annurev-med-041217-010829

Antisense oligonucleotides: absorption, distribution, metabolism, and excretion

https://www.tandfonline.com/doi/full/10.1080/17425255.2021.1992382

Antisense oligonucleotides: the next frontier for treatment of neurological disorders

https://www.nature.com/articles/nrneurol.2017.148

The powerful world of antisense oligonucleotides: From bench to bedside

https://wires.onlinelibrary.wiley.com/doi/abs/10.1002/wrna.1594

RNA-Based Therapeutics: From Antisense Oligonucleotides to miRNAs

https://www.mdpi.com/612152

Antisense oligonucleotides in neurological disorders

https://journals.sagepub.com/doi/abs/10.1177/1756286418776932%20target=

For Cancer Patients:

  • Positive RGCC test result confirming circulating tumor cells (CTCs)
  • Test must be within 6 months

For Viral or Lyme Patients:

  • Positive test confirming presence of targeted pathogen
  • PCR or antibody results accepted
  • Test must be within 6 months from a reputable laboratory

Cancer: Maximum of 4 treatments per 12-month period, spaced a minimum of 3 months apart

Viral/Lyme: Maximum of 9 treatments per 12-month period, spaced a minimum of 21 days apart

Important:

  • Q-REstrains work for a long time and can accumulate in the body and build up
  • Multiple Q-REstrain treatments cannot be given on the same day
  • No other therapies are allowed on the same day as a Q-Restrain administration

Mandatory Follow-Up Tests

  • Cancer Patients: Oncotrace or Oncotrail RGCC tests every 3-4 months to monitor CTC status and treatment effectiveness
  • Viral/Lyme Patients: Follow-up testing 4-6 months post-treatment using the same laboratory that ordered the original Q-REstrain

While generally well-tolerated, some patients may experience:

  • Mild headaches
  • Temporary increased fatigue
  • Flu-like symptoms
  • Cancer patients: Possible pain at surgical sites, risk of Tumor Lysis Syndrome with large tumors
  • Viral/Lyme patients: Herxheimer-type reactions, potential co-infection flares

Absolute Contraindications: 

  • Pregnancy or breastfeeding 
  • Recent blood transfusion 
  • Recent chemotherapy or radiotherapy (must wait 21 days) 
  • Radioactive seed therapy (permanent contraindication for cancer) 
  • Delta T-Cell therapy (permanent contraindication for cancer) 

Age Restrictions: 

  • Cancer treatment: Children under 12 
  • Viral/Lyme treatment: Children under 5 

Special Considerations 

Patients with large tumor burden require careful evaluation for Tumor Lysis Syndrome risk before treatment.

Patients should consult with their RGCC Practitioner about other potential contraindications.

Why choose Q-REstrain?

Precision Personalization: Every Q-REstrain therapy is uniquely designed for your specific genetic profile—no one-size-fits-all approach to personalized therapy and cancer.

Long-Lasting Action: A single treatment works continuously for up to six months, providing sustained therapeutic benefit through advanced gene silencing.

Cutting-Edge Science: Utilizes the latest RNA interference technology backed by thousands of safety studies in cancer personalized therapy.

Clinical Outcomes

Q-REstrain therapy demonstrates remarkable success rates across different conditions:

Cancer Patients: 78% positive clinical outcome (complete response, partial response, or stable disease)
Virus-Infected Patients: 91% positive clinical outcome
Lyme Disease Patients: 95% positive clinical outcome

Clinical outcomes are defined as complete response, partial response, or disease stabilization. Individual results may vary, and success encompasses any positive response, from complete eradication to disease stabilization.

Why choose Oncotrail?

Oncotrail has undergone rigorous evaluation to ensure high sensitivity and specificity, making it an invaluable tool for diagnostic purposes.

Through high-precision techniques, the test is used to monitor the effectiveness of a particular cancer treatment. This would objectively provide information on how well the treatment is going.

The non-invasive tracking of the cancer status would notify a treating physician whether to adjust current management or stay the course. This would be important to know in almost real-time rather than to find out much later that a treatment doesn't apply to a particular person.

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