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Understanding the mechanism of action of Mod GRF 1-29 involves delving into its interaction with the bodys biological systems and the specific pathways it influences
Ethical approval This work was approved by the regional ethics committee, CEI GIRONA, under the code name of GENOGIR
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It is an investigational medicinal product (IMP) and has not received a marketing authorisation from the Medicines and Healthcare products Regulatory Agency (MHRA)
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As a result, the medication levels can increase in the blood and lead to toxic side effects (5)
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