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Ukraine: Therapeutic / Stem Cell

Determined: No Unique Regulations*

Gene therapies permitted through existing medical drug laws.

No laws specifically regulate gene therapies, but they are regulated through existing medical drug laws overseen by the Ministry of Health, which oversees clinical trials and medical drug approval. Any facilities that store cells and other human tissues and medical staff involved in clinical trials and treatments must follow regulations developed by the Ministry of Health.

There are multiple stem cell clinics that advertise treatments for Parkinson’s disease, autism, arthritis and other conditions, but the effectiveness and safety of these treatments is questionable.

A Ukrainian physician who oversees a private fertility clinic that reportedly has done multiple mitochondrial replacement therapies (MRT, aka ‘three parent births’), a form of gene therapy that can help women whose IVF treatments have failed have a baby, has come under criticism. [See Ukraine: Germline/Embryonic]

Products/Research

  • ALS: Researchers from Cell Therapy Center EmCell used a combination of stem cell treatment and an exercise regimen to help those with ALS, a progressive degenerative disease that causes paralysis, slow the progression of their disease.

Regulatory Timeline

2002: Council of Europe’s 1997 Oviedo Convention signed, which bans all interventions and modifications in the human germline and the creation of human embryos for research. Ukraine has not ratified the convention.

NGO Reaction

None

Additional Resources

Click on a country (eg. Brazil, US) or region (eg. European Union) below to find which human / health products and processes are approved or in development and their regulatory status.

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Human / Health Gene Editing Index
Compare Regulatory Restrictions Country-to-Country

Gene editing regulations worldwide are evolving. The Gene Editing Index ratings below represent the current status of gene editing regulations and will be updated as new regulations are passed.

Colors and ratings guide
 

Regulation Status Rating
Determined: No Unique Regulations* 10
Lightly Regulated 8
Proposed: No Unique Regulations† 6
Ongoing Research, Regulations In Development 5
Highly Regulated 4
Mostly Prohibited 2
Limited Research, No Clear Regulations 1
Prohibited 0
Lightly Regulated: Gene and stem cell therapies regulated with minimal restrictions and requirements.
*Determined: No Unique Regulations: Gene and stem cell therapies regulated as phamaceuticals with no additional restrictions.

†Proposed: No Unique Regulations: Decrees under consideration for gene and stem cell therapies that would not require unique regulations beyond current restrictions on pharmaceuticals.

Therapeutic:
Gene editing of adult human cells, including gene therapy and stem cell therapy, that is used to treat and cure disease. Recent breakthroughs include CAR T-cell therapy, which uses patients’ own immune cells to treat their cancer.
Germline:
Gene editing of the human embryo or germline that results in genetic changes that are passed down to the next generation. This type of gene editing is the most controversial because changes are inherited and because it could theoretically be used to create “designer babies”. A Chinese scientist announced in 2018 that he had successfully edited twins that were brought to term. International backlash from the announcement has resulted in China and other countries working to clarify regulations on germline gene editing.

Rating by Country / Region
Click each column header and arrow to sort the countries / regions

Swipe right/left if all columns aren't visible

Country / Region Therapeutic Germline Human Rating
Japan 8 8 8
Brazil 4 0 2
Canada 4 0 2
Russia 10 5 7.5
Argentina 5 1 3
Israel 8 2 5
Australia 4 0 2
China 8 4 6
US 4 0 2
Chile 4 1 2.5
New Zealand 4 0 2
Ukraine 10 5 7.5
Central America 1 1 1
Paraguay 1 1 1
Uruguay 1 1 1
India 4 0 2
UK 4 4 4
Mexico 8 0 4
EU 4 0 2
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Gene editing is a set of techniques that can be used to precisely modify the DNA of almost any organism. It is being used for applications in human health, gene drives and agriculture. There are numerous gene-editing tools besides CRISPR-Cas 9, which gets most of the attention because it is a comparatively easy tool to use.

Gene editing does not usually involve transgenics – moving ‘foreign’ genes between species. It also refers to a specific technique in contrast to the general term GMO, which is scientifically ambiguous, as genetic modification is a process not a product. Most gene editing involves creating new products by deleting very small segments of DNA (sometimes in agriculture called Site-Directed Nuclease 1 or SDN-1 techniques), which can silence a gene or change a gene’s activity. Countries are evaluating whether or not to regulate this type of gene editing, since it is so similar to natural mutations. The GLP’s Gene Editing Index ratings reflect the regulatory status of SDN-1 techniques, which are the most liberally regulated and will generate most products in the near term.

To develop different products, gene editing can change larger segments of DNA or add DNA from other species (a form of transgenics sometimes in agriculture called SDN-2 or SDN-3 techniques). While many countries are not regulating or lightly regulating SDN-1 techniques, most are moving toward tightly regulating or even restricting SDN-2 and SDN-3.

For more background on the various gene editing SDN techniques, read background articles here and here.

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