Radioiodine Refractory Differentiated Thyroid Cancer

2

Review clinical trials related to Radioiodine Refractory Differentiated Thyroid Cancer. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Sacituzumab Tirumotecan Combined With Immunotherapy in Advanced Thyroid Cancer

This is a multicenter, open-label, multi-cohort Phase II exploratory study designed to evaluate the efficacy and safety of sacituzumab tirumotecan with or without tislelizumab in patients with unresectable, locally advanced, or metastatic anaplastic thyroid carcinoma (ATC), poorly differentiated thyroid carcinoma (PDTC), or radioactive iodine-refractory differentiated thyroid cancer (RAIR-DTC). Patients with ATC will receive sacituzumab tirumotecan in combination with tislelizumab. Patients with PDTC and RAIR-DTC will receive sacituzumab tirumotecan monotherapy. The primary objective in the ATC cohort is overall survival (OS). In the PDTC and RAIR-DTC cohorts, the primary objective is progression-free survival (PFS) assessed by investigators per RECIST v1.1.

Participants needed: 94
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Zhejiang Provincial People's HospitalUpdated: Jun 1, 2026Locations: 1
Eligibility criteria

Anaplastic thyroid carcinoma (ATC), or [+16]

Prior therapy targeting TROP2. [+18]

Status: Recruiting

Study of 177Lu-LNC1004 Injection in FAP-positive Radioiodine-refractory Differentiated Thyroid Cancer

177Lu-LNC1004 Injection, a radiopharmaceutical targeting FAP, has demonstrated preliminary antitumor effect in advanced FAP-positive solid tumor patients. The primary purpose of this study is to evaluate the efficacy of 177Lu-LNC1004 Injection in patients with FAP-positive RAIR-DTC who have failed first-line TKIs treatment or refuse standard treatment. All subjects will receive 80 mCi (± 10%) 177Lu-LNC1004 Injection intravenously every 6 weeks for 2 cycles.

Participants needed: 20
Trial details
Phase: Early Phase 1Age: 18-85Biological sex: AllType: InterventionalSponsor: Peking Union Medical College HospitalUpdated: Apr 15, 2025Locations: 1
Eligibility criteria

Subject must have the ability to understand and sign an approved informed consen... [+11]

Subject without clinical symptoms can be included in this trial after evaluation... [+21]