BioViva’s aims to be an advanced medicinal product access platform. To this end BioViva is committed to the following:

• Bridging stakeholders with biotechnology

• Accelerated path  to human trials

• Growing knowledge base

• Ensuring dependability

BioViva is a platform to expedite the development of drugs and treatments that affect human healthspan. To achieve this goal BioViva has developed a comprehensive set of biomarkers of aging, which include molecular, physiological, anatomical, clinical, and qualitative markers. BioViva also collaborates with clinicians, biomedical scientists, and statisticians to develop innovative protocols for adaptive clinical trials for gene and cells therapies. Finally, BioViva has built a bioinformatics pipeline to analyze the data generated from the biomarkers of aging in human trials and validate the treatments that are effective for treating the aging process.

BioViva has recently partnered with a patient-paid-for clinical trial company Integrated Health Systems (IHS). IHS connects doctors with patients who want to take part in paid-for clinical trials. During our collaboration with IHS, they will utilize our adaptive clinical trial protocols to conduct gene and cell therapy trials. All patients will undergo pre- and post-testing using BioViva’s comprehensive biomarkers of aging platform. Treatment efficacy and patient well being will be assessed using our bioinformatics pipeline.

The goal of BioViva is to accelerate the development of products that will effectively, and cost-efficiently treat biological aging. Our platform is designed to provide expedited and reliable feedback to our clinical and manufacturing partners, so that they may rapidly iterate their products and services to help patients improve the quality and quantity of life.

Success for BioViva entails finding therapies that work quantitatively by reversing or slowing biological aging in humans as measured by DNA methylation, metabolic, physiological, anatomical, and clinical markers. In addition, we will qualitatively improve patient well-being by helping them achieve an optimally healthy life.

BioViva is a platform for anti-aging biotech development. BioViva is to biotech, what meta-analysis is to medical research. BioViva’s platform is designed to accommodate all forms of research and development that target the aging process in humans. We work with biotech companies and biologic manufacturers and help them conduct accelerated adaptive clinical trials to ascertain the efficacy of their products in treating the aging process.

According to FDA drug approvals between 2004 and 2014, there is a 15 percent chance of going from Phase 1 through to FDA approvals for biologics, and a 7 percent chance of success for small molecules. This high rate of failure highlights the problems with preliminary drug testing platform. BioViva is a cost-effective solution for biotech companies to rapidly test their drugs in humans to determine where to embark on the expensive and time-consuming FDA or EMA approval process.

The biggest challenge in evaluating the efficacy of anti-aging treatments are biomarkers of aging. Currently, our the best biomarkers of aging are loosely associated with biological aging especially in people aged over 50.

This is clearly the biggest problem as we cannot wait for 10 years to test every treatment. Therefore at BioViva, we have designed a comprehensive biomarker of aging platform that should be able to ascertain anti-aging treatment efficacy within a couple of years.

In summary, we want to help humans live long and healthy lives, and we have built a platform to assess anyone's products that can help us achieve that goal.

BioViva’s aims to be an advanced medicinal product access platform. To this end BioViva is committed to the following:

 

• Bridging stakeholders with biotechnology

• Accelerated path  to human trials

• Growing knowledge base

• Ensuring dependability

BioViva is a platform to expedite the development of drugs and treatments that affect human healthspan. To achieve this goal BioViva has developed a comprehensive set of biomarkers of aging, which include molecular, physiological, anatomical, clinical, and qualitative markers. BioViva also collaborates with clinicians, biomedical scientists, and statisticians to develop innovative protocols for adaptive clinical trials for gene and cells therapies. Finally, BioViva has built a bioinformatics pipeline to analyze the data generated from the biomarkers of aging in human trials and validate the treatments that are effective for treating the aging process.

BioViva has recently partnered with a patient-paid-for clinical trial company Integrated Health Systems (IHS). IHS connects doctors with patients who want to take part in paid-for clinical trials. During our collaboration with IHS, they will utilize our adaptive clinical trial protocols to conduct gene and cell therapy trials. All patients will undergo pre- and post-testing using BioViva’s comprehensive biomarkers of aging platform. Treatment efficacy and patient well being will be assessed using our bioinformatics pipeline.

The goal of BioViva is to accelerate the development of products that will effectively, and cost-efficiently treat biological aging. Our platform is designed to provide expedited and reliable feedback to our clinical and manufacturing partners, so that they may rapidly iterate their products and services to help patients improve the quality and quantity of life.

Success for BioViva entails finding therapies that work quantitatively by reversing or slowing biological aging in humans as measured by DNA methylation, metabolic, physiological, anatomical, and clinical markers. In addition, we will qualitatively improve patient well-being by helping them achieve an optimally healthy life.

BioViva is a platform for anti-aging biotech development. BioViva is to biotech, what meta-analysis is to medical research. BioViva’s platform is designed to accommodate all forms of research and development that target the aging process in humans. We work with biotech companies and biologic manufacturers and help them conduct accelerated adaptive clinical trials to ascertain the efficacy of their products in treating the aging process.

According to FDA drug approvals between 2004 and 2014, there is a 15 percent chance of going from Phase 1 through to FDA approvals for biologics, and a 7 percent chance of success for small molecules. This high rate of failure highlights the problems with preliminary drug testing platform. BioViva is a cost-effective solution for biotech companies to rapidly test their drugs in humans to determine where to embark on the expensive and time-consuming FDA or EMA approval process.

The biggest challenge in evaluating the efficacy of anti-aging treatments are biomarkers of aging. Currently, our the best biomarkers of aging are loosely associated with biological aging especially in people aged over 50.

This is clearly the biggest problem as we cannot wait for 10 years to test every treatment. Therefore at BioViva, we have designed a comprehensive biomarker of aging platform that should be able to ascertain anti-aging treatment efficacy within a couple of years.

In summary, we want to help humans live long and healthy lives, and we have built a platform to assess anyone's products that can help us achieve that goal.

Overexpression of genes to suppress dsRNA innate immunity

BioViva scientist Ali Fallah et al have worked on the reprogramming potential of GCS (germline derived stem cells) the self-renewal capacity of which makes them a good source for research and clinical use, and shown that their innate immunity can be manipulated via overexpression of three key genes.

Source: NCBI Pub Med

Gene Therapy using anti-inflammatory cytokines promising against MS

 BioViva scientist Ali Fallah and his team work on novel gene therapy using anti-inflammatory cytokines and show that these can be a promising approach against multiple sclerosis (MS). 

Source:  Cell Journal.

Source of stem cells that are easily available and raise no ethical concerns→

Research by BioViva scientist Ali Fallah: " In this study, we describe an efficient approach for stable knockdown of adenosine kinase (ADK) using lentiviral system, in an astrocytoma cell line and in human Wharton’s jelly mesenchymal stem cells (hWJMSCs). These sources of stem cells besides having multilineage differentiation potential and immunomodulatory activities, are easily available in unlimited numbers, do not raise ethical concerns and are attractive for gene manipulation and cell-based gene therapy."

BioViva Supports Patient Advocacy For Gene Therapy

Alison Frase, with her son Joshua at age five in 2000, first learned about gene therapy more than 10 years ago. Sour

"Patient advocates are the driving force behind the development of many new drugs and amendments to medical regulations. It is the common man and woman who drive technology by demanding access to it. I know, because first and foremost, I am a patient advocate.

It is an absolute tragedy that Ms. Frase lost her son Joshua to X-linked myotubular myopathy. As a mother I cannot imagine anything more devastating. We all hope for a better tomorrow, but we need to realize that unless we act now, for many people, there will be no tomorrow. Each of us have a responsibility to accelerate medicine so that we can put an end to these horrible tragedies."

Liz Parrish, CEO BioViva, comments on Determined Parents are Moving the Needle on Gene Therapy