Generation of Biological Samples Positive to Somatropin for Anti-doping Control

NCT ID: NCT04042428

Last Updated: 2020-02-12

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 6 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2019-10-25
• Study Completion Date: 2020-01-08

Brief Summary

Background:

Somatropin, also known as recombinant growth hormone (rhGH), is one of the World Anti-Doping Agency (WADA) prohibited substances. Its consumption in athletes has been banned since 1990, as it is known to improve physical performance.

Hypothesis:

The subcutaneous administration of recombinant somatropin (rhGH) in healthy subjects allows obtaining positive doping samples.

The concentrations of hGH variants (isoforms) and biomarkers can be measured in serum.

Objectives:

Primary objective: To generate enough serum samples positive to recombinant somatropin in order to be analyzed as control samples by anti-doping laboratories.

Secondary objective: To determine the analytical parameters necessary to detect the administration of recombinant somatropin in healthy volunteers by direct and/or indirect methods.

Methods:

Phase I, open, randomized clinical trial, with a treatment condition (recombinant somatropin or rhGH) administered subcutaneously to 4 subjects (2:1 ratio). Control samples of the study correspond to basal samples of 2 subjects who do not receive any treatment.

Detailed Description

A blood sample volume of 450 mL is obtained from each subject receiving the treatment condition to perform the proposed tests.

In order to validate the determination methodology of hGH variants and biomarkers, blood samples from treatment group subjects are compared to reference blood samples of 450 mL from a control group (not receiving treatment) as it is not possible to obtain a basal sample of such volume from the subjects receiving treatment.

Conditions

Healthy Volunteers

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: OTHER
• Blinding Strategy: NONE

Study Groups

Treatment group

Subjects receive a 14-day treatment. A 450 mL blood sample is extracted 6 hours after the last administration (day 14).

Group Type: EXPERIMENTAL

Somatropin injection

Intervention Type: DRUG

Subjects receive a daily subcutaneous dose of 0.2 IU/kg (0.067 mg/kg) of recombinant somatropin (rhGH) during 14 days.

Control group

Subjects do not receive any treatment. A 450 mL blood sample is extracted at baseline.

Group Type: NO_INTERVENTION

No interventions assigned to this group

Interventions

Somatropin injection

Subjects receive a daily subcutaneous dose of 0.2 IU/kg (0.067 mg/kg) of recombinant somatropin (rhGH) during 14 days.

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Male volunteers between 20 and 30 years old.
• History and physical examination that demonstrate not presenting organic or psychiatric disorders.
• ECG, blood and urine tests performed before the trial within normal limits. Minor or punctual variations of these limits will be allowed if, in the opinion of the principal investigator, they have no clinical significance, do not pose a risk to the subject and do not interfere in the evaluation of the product. These variations and their non-relevance will be justified in writing.
• Body mass index [BMI: weight/height^2] between 19 and 26, and weight between 50 and 90 kg.
• Able to understand and accept the trial procedures and sign an informed consent.

• Having suffered some organic disease or major surgery during the three months prior to the trial.
• Suffering any type of illness, acute or chronic at the time of the study.
• Background or clinical evidence of cardiovascular, respiratory, renal, hepatic, endocrine, gastrointestinal, hematological, neurological, dermatological, or other acute or chronic diseases that, in the opinion of the Principal Investigator or the collaborators designated by it, may pose a risk for the subjects, may interfere with the objectives of the study, or may suggest an alteration in the absorption, distribution, metabolism or excretion of the drug.
• Having suffered some kind of bone or ligament injury in the last three years.
• History or clinical evidence of psychiatric disorders, alcoholism, drug abuse or addiction to other substances (except for nicotine) or regular consumption of psychoactive drugs. With regard to nicotine, consumers of more than 10 cigarettes/day will be excluded.
• Alcohol consumption over 15 g/day in men and 10 g/day in women.
• Consumers of more than 3 cups of coffee and/or tea per day, consumers of more than 3 units of cola, other stimulant drinks or equivalent per day, in the 2 months prior to the start of the study.
• Regular intake of medication in the month preceding the study. Other kinds of medication may be admitted at the discretion of the Investigator.
• Having donated blood or participated in studies in which there were blood draws in the previous 4 weeks.
• History of allergy, idiosyncrasy, hypersensitivity or adverse reactions to the active principle or any of the excipients. Serious adverse drug reactions.
• Having participated in another clinical trial with medication in the three months prior to the start of the study.
• Subjects with contraindications to treatment with the study drug (according to the summary of product characteristics).
• Positive serology to hepatitis B, C or HIV.
• Being unable to understand the nature, consequences of the trial and the procedures that are asked to follow.

• Minimum Eligible Age: 20 Years
• Maximum Eligible Age: 30 Years
• Eligible Sex: MALE
• Accepts Healthy Volunteers: Yes

Sponsors

Parc de Salut Mar

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Ana M Aldea Perona, Dr

Role: PRINCIPAL_INVESTIGATOR

IMIM (Hospital del Mar Medical Research Institute)

Locations

IMIM (Hospital del Mar Medical Research Institute)

Barcelona, , Spain

Countries

Spain

Other Identifiers

IMIMFTCL/GH/5

Identifier Type: -

Identifier Source: org_study_id