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Diagnosis of Pompe disease by blood Acid alpha-glucosidase (GAA) assay and GAA gene sequencing, 2. Age: 18+ years at enrollment, 3. Receiving enzyme replacement therapy (ERT) at a stable dose for >104 weeks, 4. This 24-week, Phase I/II, double-blind, randomized, placebo-controlled study investigated the safety and efficacy of extended-release albuterol in late-onset Pompe disease stably treated with enzyme replacement therapy at the standard dose for 4. 4) years and with no contraindications to intake of albuterol. Phase II Clinical Trial of Clenbuterol in Adult Patients With Pompe Disease. Phase II Clinical Trial of Clenbuterol in Adult Patients With Pompe Disease. Duke researchers conducted a 52-week, Phase 1/2 randomized study ( NCT01942590) to assess the safety and efficacy of clenbuterol in patients with late-onset Pompe disease (LOPD) who were stably treated with ERT. Researchers recruited 13 participants, 11 of whom completed the study. Correction of Biochemical Abnormalities and Improved Muscle Function in a Phase I/II Clinical Trial of Clenbuterol in Pompe Disease. Co Investigator Laura Elizabeth Case Orthopaedic Surgery, Physical Therapy. Co Investigator Priya Sunil Kishnani Pediatrics, Medical Genetics. Co Investigator Deeksha Sarihyan Bali Pediatrics, Medical Genetics. Principal Investigator Dwight D. Koeberl Pediatrics, Medical Genetics

This is an open label pilot trial in which 25 people with ALS will take clenbuterol orally at 40-80 micrograms twice daily for 24 weeks. The intervention is treatment with oral clenbuterol at 40-80 micrograms twice daily for 24 weeks. Clenbuterol (Intervention) Clinical Trials, 8 Results, Page 1. Phase II Clinical Trial of Clenbuterol in Adult Patients With Pompe Disease. CI-MPR was increased by the administration of the long-acting, selective β2-agonist clenbuterol, repurposed from the treatment of asthma to provide an adjunctive therapy in Pompe disease. Apply to this Phase 2 clinical trial treating Pompe Disease (Late-onset). Get access to cutting edge treatment via Clenbuterol, Placebos. View duration, location, compensation, and staffing details. Diagnosis of Pompe disease by blood Acid alpha-glucosidase (GAA) assay and GAA gene sequencing, 2. Age: 18+ years at enrollment, 3. Receiving enzyme replacement therapy (ERT) at a stable dose for >104 weeks, 4. Brief Summary: The goals of this study are to determine safety and efficacy with regard to motor function of oral clenbuterol in combination with ERT in subjects with LOPD Study Design Go to Resource links provided by the National Library of Medicine MedlinePlus Genetics related topics: Pompe disease Glycogen storage disease type IX https://swissprepsportsacademy.ch/groups/weight-loss-clenbuterol-clenbuterol-culturismo-total/

Originally developed to treat respiratory problems in horses, Clenbuterol is now popular among athletes and bodybuilders because of its thermogenic and lipolytic properties. When taken in the right dosage, Clenbuterol 0.04 can help you burn fat, promote muscle growth and increase energy levels. Additionally, it can boost your metabolism and suppress your appetite, making it easier to maintain a calorie deficit and achieve your fitness goals, . Clenbuterol 0.04 is available in tablet form, and the recommended dosage typically ranges from 20mcg to 120mcg per day. It is crucial to start with a low dosage and gradually increase it until you reach your optimal level.