Dose-Ranging Efficacy and Safety Study of Topical Rapamycin Cream for Facial Angiofibroma Associated With Tuberous Sclerosis Complex

Inclusion Criteria: 1. Male and female patients aged ≥ 6 years and ≤ 65 years on the day informed consent is obtained 2. Patients diagnosed with TSC based on the clinical diagnostic criteria of International Tuberous Sclerosis Complex Consensus Conference 2012 and presenting visible facial angiofibroma 3. An FA severity score of 2 or 3 on the IGA scale 4. Patients or their legal representatives capable of understanding the explanation of the clinical trial and who give written informed consent for participation 5. Patients or their legal representatives able to maintain patient diaries following the instructions of the investigator or sub-investigator Exclusion Criteria: 1. Patients who cannot carry out the treatment plan or follow-up assessment 2. Patients with serious skin lesions such as erosions or ulcers 3. Patients with known hypersensitivity to any component of the study product 4. Patients who have received rapamycin/sirolimus, everolimus, or temsirolimus within 3 months of enrolment 5. Patients who received laser therapy or surgical therapy within 6 months prior to trial enrolment 6. Patients who participated in any other clinical trial within 3 months prior to the day of enrolment 7. Patients judged unsuitable for this clinical trial by the investigator or sub-investigator 8. Pregnant or lactating females 9. Sexually active females of childbearing potential not using adequate contraception and sexually active males not using adequate contraception 10. Patients with immune dysfunction or receiving any form of immunosuppression 11. Patients with severe FA, with a score of 4 on the IGA scale 12. Patients with an FA severity score of less than 2 on the IGA scale