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HealthyEarly Phase 1hCGNCT05450900

Can Biotin Supplementation be Used to Mask hCG Abuse?

A Early Phase 1 study testing Choriogonadotropin Alpha, biotin and Microcellulose filler in people with Healthy, run by Sports Medicine Research and Testing Laboratory at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

This sponsor is an anti-doping laboratory tasked with testing athlete samples for prohibited substances by the World Anti-Doping Agency and other agencies. This study is intended to measure: 1. Read more about this study

Who is it for?
Ages 18 to 55 years, men onlyHealthy volunteers can take part
Conditions the study is for
Healthy
What is being tested?
Choriogonadotropin Alpha, biotin and Microcellulose filler
Type of treatment
Pill or oral medicine
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
10 participants
Where
1 siteUnited States
Study dates
27 Oct 2022to 2 Feb 2023
Phase
Early Phase 1
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 55 years
  • Men only
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • Participants must be healthy males aged 18 or older
  • Participants must be actively exercising individuals

Who cannot join

  • Individuals below the age of 18 or greater than the age of 55 on the day of enrollment
  • Individuals currently enrolled in a registered testing pool for anti-doping purposes
  • Individuals unwilling to provide blood or urine samples
  • Individuals that are not actively exercising
  • Individuals currently using testosterone or undergoing hypogonadism or hypoandrogenism treatment, or have within the previous 3 months
  • Individuals at risk for testicular or prostate cancer, as determined by the physician, or with a history of hormone dependent tumors of the reproductive tract and accessory organs (such as prostatic carcinoma, testicular cyst, or breast cancer)
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  • Individuals that show a high risk of heart attack, blood clots or cardiovascular disease, as defined by the physician, or who are currently using anticoagulant medications
  • Individuals with a history of cardiac, renal or hepatic disease, as defined by the physician
  • Individuals with a history of prostatic hyperplasia, venous thromboembolism, stroke, edema, or sleep apnea
  • Individuals that are diabetic or are currently taking a diabetic medicine
  • Individuals with epilepsy
  • Individuals with a known allergy to hamster protein or with hypersensitivity to hCG preparations or excipients
  • Individuals with a history of aggressive behavior or suicidality

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Sports Medicine Research and Testing Laboratory

    Salt Lake City, Utah, 84095

Other trials in United States

About this study

This sponsor is an anti-doping laboratory tasked with testing athlete samples for prohibited substances by the World Anti-Doping Agency and other agencies.

This study is intended to measure:

  1. Urinary/serum hCG (human chorionic gonadotropin) and urinary biotin concentrations in both treatment groups before, during, and after hCG intervention using standard immunoassay methods
  2. To monitor hCG in both treatment groups before and after diafiltration of urine samples prior to analysis
  3. To compare urinary and serum detectability (detection window, sensitivity) of hCG abuse in the hCG-only group compared to the hCG + biotin group
Read the detailed description

hCG, or human chorionic gonadotropin, is a protein hormone primarily produced in females by trophoblast cells during early pregnancy. hCG belongs to the glycoprotein hormone (GPH) family and exists as a heterodimer with an alpha and beta subunit. Its beta subunit is unique to hCG, however, its alpha subunit is identical to that of other GPH family members, including luteinizing hormone (LH), follicular stimulating hormone (FSH), and thyroid stimulating hormone (TSH). Due to this similarity to FSH and LH, it can be used as a female fertility treatment, however, hCG can also also stimulate the production of testosterone in the male testes and is sometimes used as a treatment for certain cases of hypogonadism. Unfortunately, this activity has led to hCG abuse by male athletes as a method to increase endogenous testosterone levels despite being listed as a prohibited substance for male athletes by the World Anti-Doping Agency (WADA).

While most anti-doping testing is conducted using mass spectrometric methods, hCG testing is conducted on immunoassay platforms that utilize biotin-streptavidin binding methods (automated analyzers, ELISA). Biotin interference is a well-known confounding factor in biotin-streptavidin immunoassays. Excess biotin in urine or serum binds to streptavidin molecules lowering the sensitivity of the assay. In certain clinical tests that utilize biotin-streptavidin binding, excess biotin can impact immunoassay results in individuals supplementing with biotin at a dose as low as 5 mg/day. Biotin, or vitamin B7, is a coenzyme involved in metabolic processes related to the breakdown of macronutrients. Biotin supplementation is considered safe and non-toxic even at remarkably high doses (<300mg/day) and it is readily available over the counter. Knowing that biotin supplementation is readily available and may be widely used, it is presumable that heavy biotin supplementation may mask illicit hCG use by athletes. To overcome this interference in a clinical setting, a method utilizing streptavidin coated microparticles has been developed to deplete biotin from samples, however this method is costly and not suitable for anti-doping applications.

The goal of this study is to understand whether hCG use can be masked by over-the-counter biotin supplementation, and whether the diafiltration method identified by Sobolevsky and Ahrens is a viable protocol for increased accuracy of hCG testing in urine samples. Additionally, we aim to understand how this potential masking effect is observed in serum samples verses urine samples as biotin is primarily excreted in urine so biotin levels are typically lower in the serum when compared to urine. The study will be conducted in male participants and will include two groups: hCG +oral biotin treatment and hCG + oral placebo treatment. Participants will have seven hCG injections and will be taking an over-the-counter biotin (or placebo) supplement daily from the onset of the study until the final day, 32 days after the first injection.

Experimental Design

Study Drug choriogonadotropin alfa Dose: 250 µg (should equate to between 2000-2300 IU), 2X per week, subcutaneously

Dietary Supplement:

Biotin (20mg), 1x per day, p.o.

Placebo Supplement:

Capsules provided by pharmacy, 1x per day, p.o.

Study Design

Subjects will be divided into two treatment groups:

Cohort 1: hCG treatment, oral biotin supplement Cohort 2: hCG treatment, oral placebo supplement As enrollment occurs, participants will be randomized evenly into one of the two cohorts in 'every other' fashion.

Conditions
Healthy
Being tested
Choriogonadotropin Alpha, biotin, Microcellulose filler

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Choriogonadotropin AlphaDrug

    Also called ovidrel, hCG

    drug, active

  • biotinDietary supplement

    Also called vitamin B7

    supplement, oral

  • Microcellulose fillerOther

    Also called placebo, capsules

    supplement, oral

Study groups in NCT05450900
Study groupRoleWhat they receive
Cohort 1Active comparatorhCG plus biotin supplement
Receives: Drug: Choriogonadotropin Alpha; Dietary Supplement: biotin
Cohort 2Placebo comparatorhCG plus placebo supplement
Receives: Drug: Choriogonadotropin Alpha; Other: Microcellulose filler

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. 1. Urinary hCG and biotin concentrations

    Urinary hCG concentration will be measured on different analytical platforms (Abbott, Roche, Siemens) that are dependent or not dependent on biotin-streptavidin chemistry for hCG measurement. Urinary biotin concentration will be measured using mass spectrometric techniques. Measured hCG concentrations, especially those during and after the dosing of Ovidrel, will be assessed in combination with the biotin concentration to understand the masking effect of biotin on urinary hCG measurement as it relates to anti-doping.

    Measured: 6 months

  2. 2. HPT-related hormone measurements in serum; biotin measurements in serum

    hCG, LH (luteinizing hormone), FSH (follicle stimulating hormone), testosterone, SHBG (sex hormone binding globulin), and estradiol will be measured in serum before and after treatment with Ovidrel. Changes in each of these compounds will be compared to individual baseline values established prior to Ovidrel use to understand the drug effects. hCG and LH will be measured on analytical platforms known to be affected by biotin interference, and all analytes (including hCG and LH) will be measured on an analytical platform not affected by biotin interference.

    Measured: 6 months

Secondary outcomes (3)
  1. 1. Detection window of hCG following use

    The length of time (following Ovidrel use) that hCG is detectable in urine will be assessed. This will be measured across different analytical platforms and in the presence and absence of biotin supplementation.

    Measured: 6 months

  2. 2. Urinary testosterone/epitestosterone ratio measurement

    The concentrations of testosterone and epitestosterone will be measured using mass spectrometric techniques; results will be compared against measurements obtained at baseline (prior to beginning the Ovidrel dosing).

    Measured: 6 months

  3. 3. CBC measurements as they relate to the Athlete Biological Passport

    Changes from individually established baselines will be assessed for the following complete blood count analytes following Ovidrel dosing: red blood cell count (RBC), hemoglobin concentration (HGB), hematocrit (HCT), mean corpuscular volume (MCV), mean corpuscular hemoglobin (MCH), mean corpuscular hemoglobin concentration (MCHC), red cell distribution width (RDW), platelet count (PLT), reticulocyte number (RET%), reticulocyte count (RET#), and immature reticulocyte fraction percent (IRF%).

    Measured: 6 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted11 Jul 2022
  2. Study start27 Oct 2022
  3. Primary completion2 Feb 2023
  4. Study completion2 Feb 2023

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Early Phase 1
Primary purpose
Other
Allocation
Randomised
Intervention model
Parallel groups
Model description
One cohort receives active drug ovidrel plus biotin supplementation One cohort receives active drug ovidrel plus a placebo
Masking
Single blind
Who is masked
Participant
Enrolment
10 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05450900
Sponsor's protocol ID
SMRTL-2022_01
Acronym
hCG
Status last verified
Feb 2023
First submitted
5 Jul 2022
Last updated
3 Feb 2023
Results posted
No
Data monitoring committee
No
FDA-regulated drug
Yes
FDA-regulated device
No
Individual data sharing
No

Publications

  • Goodrum JM, Nair VS, Moore C, Crouch AK, Eichner D, Miller GD. Impact of Biotin Supplementation on Human Chorionic Gonadotropin Immunoassays Utilizing Biotin-Streptavidin Binding Methods in Urine. Clin Chem. 2023 Jul 5;69(7):754-762. doi: 10.1093/clinchem/hvad060.

    PubMed 37253044

Questions about this trial

What is this clinical trial studying?

A Early Phase 1 study testing Choriogonadotropin Alpha, biotin and Microcellulose filler in people with Healthy, run by Sports Medicine Research and Testing Laboratory at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 2 inclusion and 13 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 3 Feb 2023. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Early Phase 1 (sometimes called Phase 0) studies give a very small amount of a treatment to a few people, mainly to see how the body handles it.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

1. Urinary hCG and biotin concentrations (time frame: 6 months). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT05450900, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 3 Feb 2023.

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