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174Cases

2021-11-01 - 2027-03-20

Phase I/II

Active
A Phase 1/1b/2 Study Evaluating the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Efficacy of AMG 193 Alone and in Combination With Docetaxel in Subjects With Advanced MTAP-null Solid Tumors
  • Condition/Disease

    Advanced MTAP-null Solid Tumors

  • Test Drug

    錠劑

Participate Sites
4Sites

Recruiting4Sites

2025-09-01 - 2031-08-14

Phase I/II

Not yet recruiting
A Phase Ib/II, Multi-site, Open-label, Two-part Trial to Evaluate the Efficacy, Safety, Pharmacokinetics, and Recommended Combination Dose of BNT324 With BNT327 in Participants With Advanced Lung Cancer
  • Condition/Disease

    Advanced Lung Cancer

  • Test Drug

    Intravenous infusion solution powder

Participate Sites
5Sites

Recruiting5Sites

2024-01-22 - 2027-05-27

Phase III

Active
A Randomized, Double-Blind, Placebo-Controlled, Multi-Regional Phase III Clinical Study of Toripalimab Alone or in Combination With Tifcemalimab (JS004/TAB004) as Consolidation Therapy in Patients With Limited-Stage Small Cell Lung Cancer Without Disease Progression Following Chemoradiotherapy
  • Condition/Disease

    Limited-Stage Small Cell Lung Cancer Without Disease Progression Following Chemoradiotherapy

  • Test Drug

    injection

Participate Sites
12Sites

Not yet recruiting1Sites

Recruiting11Sites

2023-02-01 - 2026-12-31

Phase III

Active
ROSY-T: Roll Over StudY for Patients Who Have Completed a Previous Oncology Study With Osimertinib and Are Judged by the Investigator to Clinically Benefit From Continued Treatment
  • Condition/Disease

    Cancer

  • Test Drug

    TAGRISSO (泰格莎膜衣錠)

Participate Sites
6Sites

Recruiting6Sites

2021-10-01 - 2027-12-31

Phase I/II

Completed
  • Condition/Disease

  • Test Drug

Participate Sites
7Sites

Recruiting7Sites

2025-10-01 - 2028-12-31

Phase I/II

Not yet recruiting
針對錯配修復功能(pMMR)/非微衛星高度不穩定(non-MSI-H)之局部晚期或轉移性大腸直腸癌(mCRC)患者,評估ABT301併用Tislelizumab與Bevacizumab的安全性與療效之開放性.多中心.第一/二期臨床試驗
  • Condition/Disease

    第 1 部分:*評估在 pMMR/non-MSI-H 大腸直腸癌患者中,遞增劑量的 ABT-301 與固定劑量的 Tislelizumab(200 mg,靜脈輸注)和 Bevacizumab(7.5 mg/kg,靜脈輸注,每 3 週一次)合併使用時的安全性及耐受性。*確定 ABT-301 的最大耐受劑量 (MTD) 並選擇其建議的第二期劑量 (RP2D)。第 2 部分:*評估兩種劑量/方案的 ABT-301 與 Tislelizumab 和 Bevacizumab 合併使用的療效。

  • Test Drug

    膠囊劑 靜脈輸注液 靜脈輸注液

Participate Sites
7Sites

Recruiting7Sites

2022-11-30 - 2027-03-31

Phase I/II

Completed
Phase 1/2, Open-label, Dose Escalation and Dose Expansion Study of TransCon TLR7/8 Agonist Alone or in Combination With Pembrolizumab in Participants With Locally Advanced or Metastatic Solid Tumor Malignancies
  • Condition/Disease

    Advanced Solid Tumor

  • Test Drug

    注射劑 注射液

Participate Sites
4Sites

Recruiting4Sites