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AlopeciaPhase 1/2NCT05210452

Treatment of Alopecia Using Follicular Stem Cells

A Phase 1/2 study testing Follicular stem cells and Standard treatment according to the clinical protocols in people with Alopecia, run by Institute of Biophysics and Cell Engineering of National Academy of Sciences of Belarus.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

Treatment of alopecia using the injections of cultured stem cells from human hair follicles,(which contain epithelial and mesenchymal cells stem cell) Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Alopecia
What is being tested?
Follicular stem cells and Standard treatment according to the clinical protocols
Could I receive a placebo?
No, everyone receives an active treatment
How many people
30 participants
Where
No sites listed yet
Study dates
1 Mar 2022to 31 Dec 2023
Phase
Phase 1/2
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 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Clinical diagnosis of alopecia areata, androgenic alopecia and other non-scarring hair loss
  • The patient can read, understand, follow the examination procedures and complete, if necessary, the required documentation
  • Written informed consent

Who cannot join

  • Acute or chronic diseases in the stage of decompensation
  • Chronic infectious diseases: HIV, viral hepatitis B, C, tuberculosis
  • Patients who are pregnant, breastfeeding, or fertile patients who are not using adequate contraceptive methods
  • Chronic and protracted mental disorders, all diseases with the presence of the syndrome of dependence on alcohol, drugs and psychoactive substances, any other condition that makes the patient unable to understand the nature, extent and possible consequences of the study or, in the opinion of the researcher, prevents the patient from observing and performing protocol
  • Patients are unable or unwilling to give written informed consent and / or follow research procedures
  • Any other medical condition that, in the opinion of the investigator, may be associated with an increased risk to the patient or may affect the outcome or evaluation of the study

Trial locations and contacts

No sites are listed yet.

Zinaida Kvacheva contact

+375173332223

kvachzb@tut.by

About this study

Treatment of alopecia using the injections of cultured stem cells from human hair follicles,(which contain epithelial and mesenchymal cells stem cell)

Read the detailed description

The aim of the project is to develop a biomedical cell product based on and stem progenitor cells of the hair follicle and dermal papilla, to study its efficacy in the treatment of alopecia.

Conditions
Alopecia
Being tested
Follicular stem cells, Standard treatment according to the clinical protocols
Medical subject headings
Alopecia

What participants receive

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

  • Follicular stem cellsBiological

    Cultured autologous follicular stem cells

  • Standard treatment according to the clinical protocolsOther

    Standard treatment of alopecia according to the clinical protocols

Study groups in NCT05210452
Study groupRoleWhat they receive
Patients with alopecia receiving standard treatment and follicular stem cellsExperimentalPatients with alopecia receiving standard treatment and autologous follicular stem cells
Receives: Biological: Follicular stem cells; Other: Standard treatment according to the clinical protocols
Patients with alopecia receiving standard treatmentActive comparatorPatients with alopecia receiving standard treatment
Receives: Other: Standard treatment according to the clinical protocols

What is being measured

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

  1. Number of cured patients

    Number of cured patients with significant clinical improvement

    Measured: 6 month

  2. Number of cured patients

    Number of cured patients with significant clinical improvement

    Measured: 1 year

Timeline

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

  1. First posted27 Jan 2022
  2. Study start1 Mar 2022 (estimated)
  3. Primary completion31 Dec 2023 (estimated)
  4. Study completion31 Dec 2023 (estimated)

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
Phase 1/2
Primary purpose
Treatment
Allocation
Non-randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
30 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05210452
Sponsor's protocol ID
IBCE_FollCells
Status last verified
Jan 2022
First submitted
14 Jan 2022
Last updated
27 Jan 2022
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A Phase 1/2 study testing Follicular stem cells and Standard treatment according to the clinical protocols in people with Alopecia, run by Institute of Biophysics and Cell Engineering of National Academy of Sciences of Belarus.

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 3 inclusion and 6 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: status not confirmed, as of the sponsor's last update on 27 Jan 2022. Status can change between updates, so confirm with the study contact before making plans.

What are the possible benefits and risks?

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

What does this combined phase mean?

Phase 1 studies test a treatment in a small group of people for the first time or in a new way, mainly to check safety and find the right dose.

Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.

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

Are results available for this study?

Results are not available in the source record.

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

Contact Zinaida Kvacheva (+375173332223, kvachzb@tut.by), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Number of cured patients (time frame: 6 month). 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?
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 27 Jan 2022.

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