- ICH GCP
- EU Clinical Trials Registry
Latest Trials
EudraCT Number: 2022-001796-14 | Sponsor Protocol Number: CYTB323G12101 | Start Date: 2023-03-20 | |||||||||||
Sponsor Name: Novartis Pharma AG | |||||||||||||
Full Title: An open-label, multi-center, phase 1/2 study to assess safety, efficacy and cellular kinetics of YTB323 in participants with severe, refractory systemic lupus erythematosus. | |||||||||||||
Medical condition: Systemic Lupus Erythematosus Lupus Nephritis | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Ongoing) ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-004079-17 | Sponsor Protocol Number: COMBATARF | Start Date: 2023-03-20 | |||||||||||
Sponsor Name: Rigshospitalet | |||||||||||||
Full Title: Efficacy and safety of 72-hour infusion of Prostacyclin (1 ng/kg/min) in mechanically ventilated patients with infectious pulmonary endotheliopathy – a multicentre randomized, placebo-controlled, b... | |||||||||||||
Medical condition: Infectious pulmonary endotheliopathy | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-002194-28 | Sponsor Protocol Number: NL81713.078.22 | Start Date: 2023-03-20 | |||||||||||
Sponsor Name: Erasmus MC | |||||||||||||
Full Title: Phase I/II study to determine the safety, immunogenicity and efficacy of Therapeutic Hepatitis B Virus Synthetic Long Peptide Vaccination (HEB-PEP-Study) | |||||||||||||
Medical condition: HBeAg negative chronic HBV | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-002966-34 | Sponsor Protocol Number: TAK-861-2002 | Start Date: 2023-03-20 | |||||||||||
Sponsor Name: Takeda Development Center Americas, Inc. | |||||||||||||
Full Title: A Randomized, Double-blind, Placebo-Controlled Study to Evaluate the Efficacy, Safety, and Tolerability of TAK-861 for the Treatment of Narcolepsy Without Cataplexy (Narcolepsy Type 2) | |||||||||||||
Medical condition: Narcolepsy without Cataplexy (Type 2) | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NO (Completed) SE (Ongoing) FR (Ongoing) IT (Ongoing) ES (Ongoing) FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-001951-18 | Sponsor Protocol Number: INS1009203 | Start Date: 2023-03-17 | |||||||||||
Sponsor Name: Insmed Incorporated | |||||||||||||
Full Title: An Open-Label Extension Study to Assess the Safety, Tolerability, and Effectiveness of the Long-Term use of Treprostinil Palmitil Inhalation Powder in Participants with Pulmonary Arterial Hypertension | |||||||||||||
Medical condition: Participants with Pulmonary Arterial Hypertension | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Ongoing) ES (Ongoing) DK (Ongoing) IT (Ongoing) AT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-005169-41 | Sponsor Protocol Number: SL-372A | Start Date: 2023-03-16 | |||||||||||||||||||||
Sponsor Name: ROXALL Medizin GmbH | |||||||||||||||||||||||
Full Title: Phase II-III study to assess efficacy and safety of sublingual immunotherapy in patients suffering from house dust mite allergy | |||||||||||||||||||||||
Medical condition: Patients with house dust mites related allergic rhinitis/rhinoconjunctivitis and well-controlled mild-to-moderate or without asthma | |||||||||||||||||||||||
|
|||||||||||||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-003885-19 | Sponsor Protocol Number: NOT-APPLICABLE-HUFA | Start Date: 2023-03-15 | ||||||
Sponsor Name: | ||||||||
Full Title: ECOGUIDED GENICULAR NERVE BLOCK IN PATIENTS WITH KNEE OSTEOARTHRITIS BY LOCAL ANESTHETIC OR BY COMBINATION OF LOCAL ANESTHETIC AND CORTICOID: PLACEBO-CONTROLLED RANDOMIZED BLIND CLINICAL TRIAL | ||||||||
Medical condition: KNEE OSTEOARTHRITIS | ||||||||
|
||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||
Trial protocol: ES (Ongoing) | ||||||||
Trial results: (No results available) |
EudraCT Number: 2022-002593-89 | Sponsor Protocol Number: TV48574-IMM-20038 | Start Date: 2023-03-15 | ||||||||||||||||
Sponsor Name: Teva Branded Pharmaceutical Products R&D, Inc. | ||||||||||||||||||
Full Title: A 24-Week, Phase 2b, Randomized, Double-Blind Long-Term Extension Study to Evaluate Pharmacokinetics, Efficacy Safety, and Tolerability of TEV-48574 in Adult Patients with Moderate to Severe Ulcera... | ||||||||||||||||||
Medical condition: Moderate to severe Ulcerative colitis or moderate to severe Crohn's disease | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Ongoing) CZ (Ongoing) SK (Ongoing) IT (Ongoing) BG (Ongoing) AT (Ongoing) HU (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-002540-42 | Sponsor Protocol Number: XPORT-EC-042 | Start Date: 2023-03-15 | |||||||||||||||||||||
Sponsor Name: Karyopharm Therapeutics Inc. | |||||||||||||||||||||||
Full Title: A PHASE 3, RANDOMIZED, PLACEBO-CONTROLLED, DOUBLE-BLIND, MULTICENTER TRIAL OF SELINEXOR IN MAINTENANCE THERAPY AFTER SYSTEMIC THERAPY FOR PATIENTS WITH P53 WILD-TYPE, ADVANCED OR RECURRENT ENDOMETR... | |||||||||||||||||||||||
Medical condition: Selinexor/placebo will be given as maintenance therapy after combination chemotherapy for patients with p53 wild-type, advanced or recurrent endometrial cancer | |||||||||||||||||||||||
|
|||||||||||||||||||||||
Population Age: Adults | Gender: Female | ||||||||||||||||||||||
Trial protocol: ES (Ongoing) DE (Ongoing) HU (Ongoing) BE (Ongoing) IE (Ongoing) IT (Ongoing) GR (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-003320-40 | Sponsor Protocol Number: EP-003 | Start Date: 2023-03-14 | |||||||||||
Sponsor Name: Empros Pharma AB | |||||||||||||
Full Title: A 26-week, double-blind, randomized study in participants with overweight or obesity investigating the added contribution of acarbose in EMP16 on efficacy, safety and tolerability | |||||||||||||
Medical condition: Obesity | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: (No results available) |