Clinical trials
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Ovarian – Platinum Resistant
Read more: Ovarian – Platinum ResistantThis is a Phase 1b open-label, multicenter study, evaluating the safety, tolerability, preliminary clinical activity, pharmacokinetics (PK), and pharmacodynamics of ZN-c3 in combination with other drugs.
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Lung Cancer PD-L1 <50% 1st line met
Read more: Lung Cancer PD-L1 <50% 1st line metThis study is designed to assess the efficacy and safety of datopotamab deruxtecan (Dato-DXd) in combination with pembrolizumab versus pembrolizumab in combination with pemetrexed and platinum chemotherapy in participants with no prior therapy for advanced or metastatic non-squamous non-small cell lung cancer (NSCLC).
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Breast ER+/HER2- 2nd line met
Read more: Breast ER+/HER2- 2nd line metThis phase 3 clinical study compares the safety and efficacy of OP-1250 to the standard of care options of fulvestrant or an aromatase inhibitor in women and men with breast cancer whose disease has advanced on at least one endocrine therapy in combination with a CDK4/6 inhibitor.
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Lung Cancer PD-L1 ≥50% 1st line met
Read more: Lung Cancer PD-L1 ≥50% 1st line met -
Breast ER+/Her2- Early Stage
Read more: Breast ER+/Her2- Early StageThis is a Phase III, global, randomized, open-label, multicenter, study evaluating the efficacy and safety of adjuvant giredestrant compared with endocrine therapy of physician’s choice in participants with medium- and high-risk Stage I-III histologically confirmed estrogen receptor (ER)-positive and human epidermal growth factor receptor 2 (HER2)-negative early breast cancer.
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Breast Her2+ 1st line met
Read more: Breast Her2+ 1st line metThis study is being done to see if tucatinib works better than placebo when given with other drugs to treat participants with HER2-positive breast cancer. A placebo is a pill that looks the same as tucatinib but has no medicine in it. This study will also test what side effects happen when participants take this…
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Breast TNBC PDL1- 1st line met
Read more: Breast TNBC PDL1- 1st line metThe primary objective of this study is to compare the progression-free survival (PFS) between sacituzumab govitecan-hziy (SG) versus treatment of physician’s choice (TPC) in participants with previously untreated, locally advanced, inoperable or metastatic triple-negative breast cancer whose tumors do not express programmed cell death ligand 1 (PD-L1) or in participants previously treated with anti-programmed cell…