Granulomatous Lobular Mastitis

2

Review clinical trials related to Granulomatous Lobular Mastitis. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Tocilizumab for the Treatment of Refractory Granulomatous Lobular Mastitis

Non-Lactational Granulomatous Lobular Mastitis (NL-GLM) is an inflammatory disease of unknown etiology, characterized clinically by local breast masses, accompanied by redness and swelling of the overlying skin, sinus tract formation, and other symptoms. Currently, there is no universally accepted standard treatment for this condition; previous expert consensus or practice guidelines have mostly recommended systemic glucocorticoid therapy as the primary treatment approach. Our team's preliminary research has confirmed that local glucocorticoid injection achieves efficacy equivalent to systemic administration but with better safety, making it a first-line treatment option for NL-GLM. However, in our preliminary studies and literature reports, we found that some patients still exhibit glucocorticoid dependence or resistance (i.e., refractory NL-GLM) after receiving either local or systemic glucocorticoid therapy. The lack of high-quality evidence to support subsequent-line treatments has become a major bottleneck in clinical management. Additionally, some patients cannot tolerate glucocorticoid therapy due to its adverse effects. Research has shown that the IL-6 inflammatory pathway is significantly activated in the lesion tissues and peripheral blood of NL-GLM patients, and the IL-6 inhibitor tocilizumab has demonstrated efficacy in various autoimmune diseases. Based on this, this study intends to conduct a dual-center, single-arm clinical trial to systematically evaluate the efficacy and safety of tocilizumab in the treatment of refractory NL-GLM. The aim is to fill the treatment gap, provide high-level evidence for clinical practice, and ultimately improve patient outcomes.

Participants needed: 31
Trial details
Phase: Phase 1, Phase 2Age: 20-50Biological sex: FemaleType: InterventionalSponsor: Sun Yat-Sen Memorial Hospital of Sun Yat-Sen UniversityUpdated: May 19, 2026
Eligibility criteria

Females aged 20 to 50 years; [+4]

Bilateral mastitis occurring simultaneously or sequentially within six months. [+29]

Status: Not yet recruiting

Efficacy and Safety of Sanyong Jiedu Granules in Treating Lumps-Type Non-Lactational Mastiti

To evaluate the efficacy and safety of Sanyong Jiedu Granules in treating non-lactational mastitis with lump formation, and to investigate the relationship between its clinical efficacy and treatment duration.

Participants needed: 210
Trial details
Age: 20-50Biological sex: FemaleType: InterventionalSponsor: Caigang LiuUpdated: Apr 6, 2026Locations: 1
Eligibility criteria

Women aged 20-50 years (inclusive) who are not in lactation or pregnancy (as con... [+4]

Patients with intolerance or poor compliance to the investigational drug, or kno... [+5]