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28Cases

2024-07-01 - 2030-12-31

Phase II

Active
  • Condition/Disease

  • Test Drug

Participate Sites
3Sites

Recruiting3Sites

2023-08-10 - 2026-12-31

Phase I

Active
A Phase 1, Open-label, Multicenter Study to Assess Safety, Tolerability, PK, and Efficacy of MK-1084 as Monotherapy and as Part of Various Combination Therapies in Participants With KRAS G12C Mutant Advanced Solid Tumors
  • Condition/Disease

    Advanced Solid Tumors

  • Test Drug

    MK-1084 Gisuda Injection

Participate Sites
3Sites

Recruiting3Sites

2025-02-01 - 2033-12-31

Phase II

Completed
A Phase 2, Umbrella Study to Evaluate the Safety, Tolerability, and Clinical Activity of Investigational Agents for Newly Diagnosed, High-Risk, Early-Stage Triple-Negative Breast Cancer
  • Condition/Disease

    Early Triple Negative Breast Cancer

  • Test Drug

    注射劑 注射劑

Participate Sites
3Sites

Recruiting3Sites

2024-10-01 - 2028-06-30

Phase III

Active
  • Condition/Disease

  • Test Drug

Participate Sites
5Sites

Recruiting5Sites

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

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

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