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11 Resultado(s)
Ensaio em fase de recrutamento = ; Ensaio a decorrer =
; Financiado por um membro do IRDiRC =
; Membro de uma ERN =
Ensaio (s) clínico (s) nacional (is)

AUSTRIA
WIEN
ADDRESS: NOT PROVIDED - AT

An Open-label, Multi-center, Roll-over Study to Assess Long Term Safety in Patients With Endogenous Cushing's Syndrome Who Have Completed a Prior Novartis-sponsored Osilodrostat (LCI699) Study and Are Judged by the Investigator to Benefit From Continued Treatment With Osilodrostat (Phase 2) - AT
Institution: Information not provided - AT

AUSTRIA
WIEN
ADDRESS: NOT PROVIDED - AT

GRACE: Glucocorticoid Receptor Antagonism in the Treatment of Cushing Syndrome: A Phase 3, Double-Blind, Placebo-Controlled, Randomized-Withdrawal Study of the Efficacy and Safety of Relacorilant - AT
Institution: Information not provided - AT

BELGICA
ARRONDISSEMENT BRUSSELS-CAPITAL
BRUSSELS

A Phase II, Multicenter, Open-label, Non-comparative Study to Evaluate the Pharmacokinetics, Pharmacodynamics, and Tolerability of Osilodrostat in Children and Adolescent Patients With Cushing's Disease - BE
Universitair Ziekenhuis Brussel
Endocrinologie

ESPANHA
Andalucía
MÁLAGA

An Open-Label Extension Study of the Safety of Relacorilant (CORT125134) in the Treatment of the Signs and Symptoms of Endogenous Cushing Syndrome (Phase II-III) - ES
Hospital Universitario Virgen de la Victoria

ESPANHA
Andalucía
SEVILLA

An Open-Label Extension Study of the Safety of Relacorilant (CORT125134) in the Treatment of the Signs and Symptoms of Endogenous Cushing Syndrome (Phase II-III) - ES
Hospital Universitario Virgen del Rocío

ESPANHA
Cataluña
GIRONA

An Open-Label Extension Study of the Safety of Relacorilant (CORT125134) in the Treatment of the Signs and Symptoms of Endogenous Cushing Syndrome (Phase II-III) - ES
Hospital Universitari de Girona Dr. Josep Trueta

ESPANHA
Madrid
ADDRESS: NOT PROVIDED - ES

GRACE: Glucocorticoid Receptor Antagonism in the Treatment of Cushing Syndrome: A Phase 3, Double-Blind, Placebo-Controlled, Randomized-Withdrawal Study of the Efficacy and Safety of Relacorilant - ES
Institution: Information not provided - ES

ESPANHA
Madrid
ADDRESS: NOT PROVIDED - ES

An Open-label, Multi-center, Roll-over Study to Assess Long Term Safety in Patients With Endogenous Cushing's Syndrome Who Have Completed a Prior Novartis-sponsored Osilodrostat (LCI699) Study and Are Judged by the Investigator to Benefit From Continued Treatment With Osilodrostat - ES
Institution: Information not provided - ES

ESPANHA
Madrid
MADRID

An Open-Label Extension Study of the Safety of Relacorilant (CORT125134) in the Treatment of the Signs and Symptoms of Endogenous Cushing Syndrome (Phase II-III) - ES
Hospital General Universitario Gregorio Marañón

REINO UNIDO
Greater Manchester
ADDRESS: NOT PROVIDED - UK

A Phase 2 Randomized, Double-Blind, Placebo-Controlled Study of ATR-101 for the Treatment of Cushing's Syndrome
Institution: Information not provided - UK

BELGICA
ARRONDISSEMENT BRUSSELS-CAPITAL
BRUSSELS