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40Cases

2023-07-31 - 2026-04-19

Others

Active
A TREATMENT PROTOCOL FOR PARTICIPANTS CONTINUING FROM PFIZER-SPONSORED PALBOCICLIB CLINICAL STUDIES
  • Condition/Disease

    Breast Cancer 、Head and Neck Cancer

  • Test Drug

    膠囊劑 錠劑

Participate Sites
2Sites

Not yet recruiting1Sites

Recruiting1Sites

2024-09-01 - 2032-12-31

Phase III

Active
  • Condition/Disease

  • Test Drug

Participate Sites
5Sites

Recruiting5Sites

2024-01-01 - 2028-12-31

Others

Active
  • Condition/Disease

  • Test Drug

Participate Sites
8Sites

Recruiting8Sites

2024-07-31 - 2031-12-31

Phase III

Active
A Randomised, Open-Label, Phase III Study of Saruparib (AZD5305) Plus Camizestrant compared with Physician’s Choice CDK4/6 Inhibitor Plus Endocrine Therapy or Plus Camizestrant for the First-Line Treatment of Patients with BRCA1, BRCA2 or PALB2 Mutations and Hormone Receptor-Positive, HER2-Negative (IHC 0, 1+, 2+/ ISH non-amplified) Advanced Breast Cancer (EvoPAR-Breast01)
  • Condition/Disease

    BRCA1, BRCA2 or PALB2 Mutations and Hormone Receptor-Positive, HER2-Negative (IHC 0, 1+, 2+/ ISH non-amplified) Advanced Breast Cancer (EvoPAR-Breast01)

  • Test Drug

    tablets tablets

Participate Sites
7Sites

Recruiting7Sites

2024-10-25 - 2026-12-31

Phase I

Active
  • Condition/Disease

  • Test Drug

Participate Sites
4Sites

Recruiting4Sites

2025-06-01 - 2031-11-21

Phase III

Completed
SERENA-8:一項在雌激素受體陽性、HER2 陰性、無法手術的局部晚期或轉移性乳癌患者,且在芬香環酶抑制劑 + CDK4/6 抑制劑治療後病情出現惡化的患者
  • Condition/Disease

    依據評估以下族群的 PFS ,證明 camizestrant + capivasertib 相較於醫師選擇 ET 的優越性• 整體試驗族群和/或• 帶有 PIK3CA/AKT1/PTEN 變異的乳癌患者子族群1和/或• 未帶有 PIK3CA/AKT1/PTEN 變異的乳癌患者子族群和/或• 帶有 ESR1m 的乳癌患者子族群PFS 的定義為,自隨機分配起、直至由 BICR 按 RECIST 版本 1.1 評估為惡化或因任何原因死亡的時間。此外,在進一步補充分析中:• PFS 將由當地試驗中心試驗主持人依據 RECIST 1.1 進行評估。

  • Test Drug

    膜衣錠 膜衣錠 注射液劑

Participate Sites
4Sites

Recruiting4Sites

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