- Trials with a EudraCT protocol (6)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
6 result(s) found for: TA-8995.
Displaying page 1 of 1.
EudraCT Number: 2012-005643-24 | Sponsor Protocol Number: TA-8995-03 | Start Date*: 2013-07-29 | |||||||||||
Sponsor Name:Xention Limited | |||||||||||||
Full Title: A Multi-Centre, Randomised, Double Blind, Placebo Controlled, Parallel Group Study of TA 8995 in Patients with Mild Dyslipidaemia, Alone and In Combination with Statin Therapy | |||||||||||||
Medical condition: Mild dyslipidaemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-005092-39 | Sponsor Protocol Number: TA-8995-304 | Start Date*: 2022-08-25 | ||||||||||||||||
Sponsor Name:NewAmsterdam Pharma BV | ||||||||||||||||||
Full Title: Obicetrapib and Cardiovascular Outcomes: A Placebo-Controlled, Double-Blind, Randomized Phase 3 Study to Evaluate the Effect of 10 mg Obicetrapib in Participants With Atherosclerotic Cardiovascular... | ||||||||||||||||||
Medical condition: atherosclerotic cardiovascular disease (ASCVD) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Trial now transitioned) IT (Trial now transitioned) SK (Trial now transitioned) NL (Trial now transitioned) HU (Trial now transitioned) BG (Trial now transitioned) DK (Trial now transitioned) CZ (Trial now transitioned) FI (Trial now transitioned) LV (Trial now transitioned) ES (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-004935-22 | Sponsor Protocol Number: TA-8995-303 | Start Date*: 2020-10-01 | |||||||||||
Sponsor Name:NewAmsterdam Pharma BV | |||||||||||||
Full Title: A Placebo-Controlled, Double-Blind, Randomized Phase 2 Study to Evaluate the Effect of Obicetrapib in Combination with Ezetimibe in Participants with Mild Dyslipidemia | |||||||||||||
Medical condition: mild dyslipidemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-005064-22 | Sponsor Protocol Number: TA-8995-301 | Start Date*: 2022-09-22 | ||||||||||||||||
Sponsor Name:NewAmsterdam Pharma B.V. | ||||||||||||||||||
Full Title: Obicetrapib on Top of Maximum Tolerated Lipid-Modifying Therapies (BROOKLYN): A Placebo-Controlled, Double-Blind, Randomized, Phase 3 Study to Evaluate the Effect of 10 mg Obicetrapib in Partici... | ||||||||||||||||||
Medical condition: dyslipidemia heterozygous familial hypercholesterolemia (HeFH) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Ongoing) NL (Completed) CZ (Completed) PL (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-002687-41 | Sponsor Protocol Number: TA-8995-AD-1 | Start Date*: 2021-12-09 |
Sponsor Name:NewAmsterdam Pharma BV | ||
Full Title: A Phase 2a, Proof-of-Concept, Open-Label Study to Evaluate the Pharmacodynamics, Pharmacokinetics, and Safety of Obicetrapib in Patients with Early Alzheimer’s Disease (Hetero/Homozygote APOE4 Carr... | ||
Medical condition: Alzheimer's disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2021-005065-40 | Sponsor Protocol Number: TA-8995-302 | Start Date*: 2022-05-13 | ||||||||||||||||||||||||||
Sponsor Name:NewAmsterdam Pharma B.V. | ||||||||||||||||||||||||||||
Full Title: Obicetrapib on Top of Maximum Tolerated Lipid-Modifying Therapies (BROADWAY): A Placebo-Controlled, Double-Blind, Randomized Phase 3 Study to Evaluate the Effect of 10 mg Obicetrapib in Participant... | ||||||||||||||||||||||||||||
Medical condition: dyslipidemia heterozygous familial hypercholesterolemia (HeFH) atherosclerotic cardiovascular disease (ASCVD) | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: NL (Completed) DK (Completed) CZ (Completed) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
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