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The safety and efficacy of autologous peripheral blood mononuclear cell ex vivo culture amplified cells (MNC-QQ) for alopecia: Phase 1 / 2 clinical study

Phase 1
Recruiting
Conditions
Alopecia
Hair loss, alopecia, baldness
Registration Number
JPRN-jRCTb030230286
Lead Sponsor
Ikeda Yoshio
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
5
Inclusion Criteria

1. Patients with written informed consent.
2. Patiens are at the age of 18 to 75 at the time of informed consent.
3. Patients affected alopecia and want to receive regenerative therapy.

Exclusion Criteria

1. Patients with HbA1c(NGSP) more than 10.0 with the medication for diabetes.
2. Patients with systemic infection.
3. Patients with severe anemia.
4. Patients with malignancy, or within 5 years after recover from malignant tumor (10 years after breast cancer), except for cutaneous basal cell carcinoma.
5. Patients with hematopoietic disorders such as leukemia, myeloproliferative disease, marrow dysplasia syndrome.
6. Pregnant women.
7. Patients infected with HIV, active HBV, HCV, HTLV, or syphilis in screening test.
8. Patients not expect to live for a year or more.
9. Patients enrolled in any other clinical trial within 90 days before informed consent.
10. Patients who can't consent not to change medication.
11. Any other reason that the Clinical Researchers may have for considering a case unsuitable for the study.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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