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Effect of Mirabegron on promoting brown adipose tissue activation

Effect of Mirabegron on promoting brown adipose tissue activation

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200066915
Enrollment
Unknown
Registered
2022-12-21
Start date
2022-08-18
Completion date
Unknown
Last updated
2023-05-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

tumour

Interventions

health volunteers:Mirabegron p.o. 28days 100mg qd. or 200mg qd.
Tumor patients:Mirabegron p.o. 28days 100mg qd. or 200mg qd.

Sponsors

Zhejiang Provincial People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1.Sign the informed consent before the test, and fully understand the content, process and possible adverse events. 2.For health volunteer:Both men and women, aged 18-65 years (including the boundary value) . 3.For tumour patients: Both men and women, aged 18-65 years (including the boundary value),Tumor bearing and not in the period of chemotherapy and targeted drug intervention. 4.Body mass index (BMI) is 19.0–26.0 kg/m2 (including critical values). 5.Proper bone marrow and organ function, as defined below: HB=80h/LANC=1.5*109/LPLT=50*109/L;ALT=3 ULN;AST=3 ULN;AST=3 ULN;TBIL=1.5 ULN 6.The expected survival is 3 months or more.

Exclusion criteria

Exclusion criteria: a.A history of tuberculosis infection. b.Patients with contraindications to mirabegron: allergic to mirabegron or any of its excipients; Patients with poorly controlled severe hypertension (SBP?180mmHg or/and DBP?110mmHg) c.Subjects with a history of fainting bloodfainting needle. d.Unwilling to stop drinking alcohol or using any alcoholic products during the study. e.Physical examination, electrocardiogram, laboratory examination, color ultrasound, chest orthogram, vital signs and study related examination abnormalities are clinically significant (based on the clinician's judgment). f.Female subjects who used long-acting estrogen or progesterone injections or implants within 6 months prior to the study. g.Women who are pregnant or breastfeeding. h.The subject may not be able to complete the study for other reasons or may not be able to participate in the study for other reasons judged by the investigator.

Design outcomes

Primary

MeasureTime frame
The growth of brown adipose tissue;

Secondary

MeasureTime frame
blood glucose/GTT;

Countries

China

Contacts

Public ContactMinghua Ge
gemingh@163.com13605813782

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026