NL-OMON44014
Completed
Not Applicable
A randomized, double-blind, placebo-controlled study to investigate the effects of an 8-week recombinant human erythropoietin (NeoRecormon) treatment on well-trained cyclists and their cycling performance. - Erythropoetine effects on cycling performance.
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Fietsprestatie
- Sponsor
- Centre for Human Drug Research
- Enrollment
- 48
- Status
- Completed
- Last Updated
- 2 years ago
Overview
Brief Summary
Trial is onging in other countries
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\. Well\-trained (as determined by cycling history and maximal power output \>4 W/kg) male subjects, 18 to 50 years old (inclusive);
- •2\. Subjects must be healthy / medically stable on the basis of clinical laboratory tests, medical history, vital signs, and 12\-lead ECG performed at screening, including exercise ECG.
- •3\. Each subject must sign an informed consent form prior to the study. This means the subject understands the purpose of and procedures required for the study.
Exclusion Criteria
- •1\. Any clinically significant abnormality, as determined by medical history taking and physical examinations, obtained during the screening visit that in the opinion of the investigator would interfere with the study objectives or compromise subject safety.
- •2\. Unacceptable known concomitant diagnoses or diseases at baseline, e.g., known cardiovascular, pulmonary, muscle, metabolic or haematological disease, renal or liver dysfunction, ECG or laboratory abnormalities, etc.
- •3\. Unacceptable concomitant medications at baseline, e.g., drugs known or likely to interact with the study drugs or study assessments.
- •4\. Unacceptable potential cycling performance enhancing medications at baseline, e.g. Erythropoiesis\-stimulating agents, Anabolic Androgenic Steroids, Growth Hormone, Insulin, IGF\-I and Beta\-Adrenergic Agents or methods, e.g. altitude tents.
- •5\. Blood transfusion in the past three months.
- •6\. Loss or donation of blood over 500 mL within three months.
- •7\. Participation in a clinical trial within 90 days of screening or more than 4 times in the previous year.
- •8\. Known hypersensitivity to the treatment or drugs of the same class, or any of their excipients.
- •9\. Any known factor, condition, or disease that might interfere with treatment compliance, study conduct or interpretation of the results such as drug or alcohol dependence or psychiatric disease.
- •10\. Positive urine drug test at screening
Outcomes
Primary Outcomes
Not specified
Similar Trials
Completed
Phase 2
A Randomized, Double-Blind, Placebo Controlled Study of COR388 HCl in Subjects with Alzheimer*s DiseaseAlzheimer's diseasedementianeurodegenerative disease10012272NL-OMON54863Cortexyme, Inc.31
Completed
Phase 2
A randomized, double-blind, placebo controlled multiple dose study of subcutaneous ACZ885 for the treatment of abdominal aortic aneurysmAbdominal aortic aneurysmdilation of the aorta in the abdomen10002363NL-OMON38947ovartis7
Completed
Phase 2
A Randomised, Double-Blind, Placebo-Controlled Multicentre Clinical Trial of Inhaled Molgramostim in Autoimmune Pulmonary AlveoLAr Proteinosis PatientsNL-OMON46238Savara ApS9
Completed
Phase 3
A Randomized, Double-Blind, Placebo-Controlled, Parallel Group Study to Evaluate the Efficacy and Safety of SAR236553/REGN727/Alirocumab in Patients With Heterozygous Familial Hypercholesterolemia Not Adequately Controlled With Their Lipid-Modifying Therapyfamilial hypercholesterolemiainherited hyperlipidemia100274241001331710003216NL-OMON39858Sanofi-aventis18
Completed
Phase 3
A Randomized, Double-Blind, Placebo-Controlled, Parallel Group Study to evaluate the Efficacy and Safety of SAR236553 (REGN727) in Patients With Heterozygous Familial Hypercholesterolemia and LDL-C higher or equal to 160mg/dL with Their Lipid-Modifying Therapyfamilial hypercholesterolemiainherited hyperlipidemia100274241001331710003216NL-OMON39914Sanofi-aventis11