- Trials with a EudraCT protocol (10)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
10 result(s) found for: Estrogen Receptor Alpha.
Displaying page 1 of 1.
EudraCT Number: 2018-001364-27 | Sponsor Protocol Number: ZN-c5-001 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Zeno Alpha, Inc., | |||||||||||||
Full Title: A PHASE 1/2 OPEN LABEL, MULTICENTER STUDY TO ASSESS THE SAFETY, TOLERABILITY, PHARMACOKINETICS, AND ANTI-TUMOR ACTIVITY OF ZN-C5 ALONE AND IN COMBINATION WITH PALBOCICLIB IN SUBJECTS WITH ESTROGEN-... | |||||||||||||
Medical condition: Estrogen-receptor positive, human epidermal growth factor receptor-2 negative advanced breast cancer | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) LT (Ongoing) BG (Prematurely Ended) HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-002961-23 | Sponsor Protocol Number: ODO-TE-B301 | Start Date*: Information not available in EudraCT |
Sponsor Name:Odonate Therapeutics, Inc. | ||
Full Title: A Multinational, Multicenter, Randomized, Phase 3 Study of Tesetaxel plus a Reduced Dose of Capecitabine versus Capecitabine Alone in Patients with HER2 Negative, Hormone Receptor Positive, Locally... | ||
Medical condition: Patients with Breast Cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: CZ (Prematurely Ended) HU (Completed) ES (Prematurely Ended) GB (GB - no longer in EU/EEA) AT (Prematurely Ended) DE (Completed) BE (Prematurely Ended) FR (Prematurely Ended) PL (Prematurely Ended) IT (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2020-004775-40 | Sponsor Protocol Number: APD334-202EU | Start Date*: 2021-05-11 | |||||||||||
Sponsor Name:Arena Pharmaceuticals Inc. | |||||||||||||
Full Title: A Multicenter, Randomized, Double-Blind, Parallel-Group Study to Assess the Efficacy and Safety of Oral Etrasimod as Induction and Maintenance Therapy for Moderately to Severely Active Crohn’s Disease | |||||||||||||
Medical condition: Crohn's Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) DE (Ongoing) DK (Ongoing) SK (Ongoing) LT (Ongoing) LV (Completed) HU (Ongoing) CZ (Ongoing) PT (Prematurely Ended) NO (Completed) BE (Ongoing) BG (Ongoing) ES (Ongoing) HR (Ongoing) IT (Ongoing) RO (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-003600-12 | Sponsor Protocol Number: MORAb-202-G000-201 | Start Date*: 2022-07-25 | ||||||||||||||||||||||||||
Sponsor Name:Eisai Limited | ||||||||||||||||||||||||||||
Full Title: A Multicenter, Open-Label Phase 1/2 Trial Evaluating the Safety, Tolerability, and Efficacy of MORAb-202, a folate receptor alpha (FRα)-targeting antibody-drug conjugate (ADC) in Subjects With Sele... | ||||||||||||||||||||||||||||
Medical condition: Solid tumors expressing folate receptor alpha in 4 tumor types: platinum resistant ovarian cancer, triple-negative breast cancer (TNBC), endometrial cancer (EC), and non-small cell lung cancer aden... | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: FR (Trial now transitioned) ES (Ongoing) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-003656-35 | Sponsor Protocol Number: E7389-G000-211 | Start Date*: 2006-03-14 |
Sponsor Name:Eisai Limited | ||
Full Title: A phase II open label single-arm study of E7389 in patients with locally advanced or metastatic breast cancer, previously treated with anthracycline, taxane, and capecitabine therapy, refractory to... | ||
Medical condition: Locally advanced or metastatic breast cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: BE (Completed) ES (Completed) GB (Completed) AT (Completed) DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2022-003323-17 | Sponsor Protocol Number: IMP321-P016 | Start Date*: 2023-03-24 | ||||||||||||||||
Sponsor Name:Immutep S.A.S. | ||||||||||||||||||
Full Title: AIPAC-003: A randomized, double-blind, placebo-controlled Phase 3 trial testing eftilagimod alpha (soluble LAG-3) in HER2-neg/low metastatic breast cancer patients receiving paclitaxel, following a... | ||||||||||||||||||
Medical condition: HER2-neg/low metastatic breast cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-004340-11 | Sponsor Protocol Number: 17403 | Start Date*: 2018-06-13 | |||||||||||
Sponsor Name:Bayer AG | |||||||||||||
Full Title: A randomized, open label, multicenter Phase 2/3 study to evaluate the efficacy and safety of rogaratinib (BAY 1163877) compared to chemotherapy in patients with FGFR-positive locally advanced or me... | |||||||||||||
Medical condition: mRNA FGF receptor 1 and 3 positive locally advanced or metastatic urothelial carcinoma progressed after prior platinum-containing chemotherapy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) IE (Completed) NL (Prematurely Ended) FR (Completed) AT (Completed) CZ (Completed) ES (Completed) PT (Completed) FI (Completed) SK (Completed) HU (Completed) DK (Completed) BE (Completed) SE (Completed) PL (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-004207-39 | Sponsor Protocol Number: AGO-OVAR2.34 | Start Date*: 2021-06-07 | ||||||||||||||||||||||||||
Sponsor Name:AGO Research GmbH | ||||||||||||||||||||||||||||
Full Title: A randomized phase II trial of Mirvetuximab soravtansine (IMGN853), in folate receptor alpha (FRα) high recurrent ovarian cancer eligible for platinum-based chemotherapy. supported by: DIAGNOSTIC ... | ||||||||||||||||||||||||||||
Medical condition: This trial evaluates the efficacy and safety of Mirvetuximab soravtansine (IMGN853) plus Carboplatin chemotherapy in FRα high patients with recurrent ovarian cancer who are eligible for platinum-ba... | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||||||||||||
Trial protocol: DE (Ongoing) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-002217-35 | Sponsor Protocol Number: AG348-C-010 | Start Date*: 2018-11-20 | |||||||||||
Sponsor Name:Agios Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Phase 2, Open-Label, Multicenter Study to Determine the Efficacy, Safety, Pharmacokinetics, and Pharmacodynamics of AG-348 in Adult Subjects With Non-Transfusion-Dependent Thalassemia | |||||||||||||
Medical condition: Non-Transfusion-Dependent Thalassemia | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-005774-25 | Sponsor Protocol Number: SC104 | Start Date*: 2022-06-16 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:SOTIO Biotech AG | ||||||||||||||||||||||||||||||||||||||
Full Title: A phase 2, open-label, single-arm, multicenter study of SOT101 in combination with pembrolizumab to evaluate the efficacy and safety in patients with selected advanced/refractory solid tumors | ||||||||||||||||||||||||||||||||||||||
Medical condition: advanced/refractory solid tumors | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: ES (Temporarily Halted) CZ (Prematurely Ended) BE (Completed) IT (Ongoing) HU (Ongoing) PL (Completed) | ||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
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