Clinical trials

The European Union Clinical Trials Register allows you to search for protocol and results information on:

interventional clinical trials that were approved in the European Union (EU)/European Economic Area (EEA) under the Clinical Trials Directive 2001/20/EC

clinical trials conducted outside the EU/EEA that are linked to European paediatric-medicine development

EU/EEA interventional clinical trials approved under or transitioned to the Clinical Trial Regulation 536/2014 are publicly accessible through the
Clinical Trials Information System (CTIS).

The EU Clinical Trials Register currently displays 44364 clinical trials with a EudraCT protocol, of which 7388 are clinical trials conducted with subjects less than 18 years old. The register also displays information on 18700 older paediatric trials (in scope of Article 45 of the Paediatric Regulation (EC) No 1901/2006).

Phase 1 trials conducted solely on adults and that are not part of an agreed paediatric investigation plan (PIP) are not publicly available (see Frequently Asked Questions ).

Examples: Cancer AND drug name. Pneumonia AND sponsor name.
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Trials with a EudraCT protocol (44,364)
Paediatric studies in scope of Art45 of the Paediatric Regulation (18,700)

44,364 result(s) found. Displaying page 1,786 of 2,219.

EudraCT Number: 2020-001461-36

Sponsor Protocol Number: CT-AMT-130-02

Start Date*: 2021-06-30

Sponsor Name:uniQure biopharma B.V.

Full Title: A Phase Ib/II Randomised, Double-Blind Study to Explore Safety, Tolerability, and Efficacy Signals of Multiple Doses of Striatally-Administered rAAV5-miHTT Total Huntingtin Gene (HTT) Lowering Ther...

Medical condition: Huntington Disease

Disease:	Version	SOC Term	Classification Code	Term	Level
Disease:	27.1	10010331 - Congenital, familial and genetic disorders	10070668	Huntington's disease	PT

Population Age: Adults

Gender: Male, Female

Trial protocol: PL (Trial now transitioned) DE (Prematurely Ended)

Trial results: (No results available)

EudraCT Number: 2020-001578-31

Sponsor Protocol Number: CINC280A2301

Start Date*: 2020-08-26

Sponsor Name:Novartis Pharma AG

Full Title: A phase III, randomized, controlled, open-label, multicenter, global study of capmatinib versus SoC docetaxel chemotherapy in previously treated patients with EGFR wt, ALK negative, locally advance...

Medical condition: cMET mutated NSCLC

Disease:	Version	SOC Term	Classification Code	Term	Level
Disease:	21.1	10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps)	10061873	Non-small cell lung cancer	PT

Population Age: Adults, Elderly

Gender: Male, Female

Trial protocol: HU (Completed) NL (Completed) DE (Completed) PT (Completed) FR (Completed) LT (Completed) BE (Completed) IT (Prematurely Ended) BG (Prematurely Ended)

Trial results: View results

EudraCT Number: 2021-004846-39

Sponsor Protocol Number: N-20200025

Start Date*: 2023-04-26

Sponsor Name:Aalborg University Hospital

Full Title: 68Ga-PSMA PET/CT vs. 18F-PSMA PET/CT for the diagnosis of metastases in newly diagnosed high-risk prostate cancer patients undergoing radical prostatectomy

Medical condition: Prostate Cancer

Disease:	Version	SOC Term	Classification Code	Term	Level
	20.0	100000004864	10036910	Prostate cancer NOS	LLT
	21.1	100000004848	10065410	Combined positron emission tomogram and computerized tomogram	LLT

Population Age: Adults, Elderly

Gender: Male

Trial protocol: DK (Completed)

Trial results: (No results available)

EudraCT Number: 2016-002065-66	Sponsor Protocol Number: OY102016	Start Date*: 2016-11-07
Sponsor Name:Miikka Tervonen
Full Title: Intranasal dexmedetomidine sedation during intra-articular joint injections in pediatric population
Medical condition: All the patients from 1year to 18 years of age who have been diagnosed by a pediatric rheumatologist to have a joint inflammation needing intra-articular corticosteroid injection in 1 to 5 joints
Disease:
Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults		Gender: Male, Female
Trial protocol: FI (Completed)
Trial results: (No results available)

EudraCT Number: 2017-004744-38	Sponsor Protocol Number: HCA-2017-1	Start Date*: 2018-09-11
Sponsor Name:Tays Sydänkeskus Oy
Full Title: New truncal nerve blocks for upper torso. Part 1. Serratus anterior plane block (SAPB): Effect on pain and recovery after thoracoskopic lung surgery. Part 2. Subpectoral interfacial plane block (S...
Medical condition: Osa 1 (SAPB): Suurin osa keuhkoleikkauksista tehdään keuhkon, keuhkopussin tai välikarsinan muutosten takia. Osa 2 (SIP): Avosydänkirurgiset läppäleikkaukset tehdään sydänläppien vuotojen, ahtaumi...
Disease:
Population Age: Adults, Elderly		Gender: Male, Female
Trial protocol: FI (Completed)
Trial results: (No results available)

EudraCT Number: 2020-004802-70	Sponsor Protocol Number: APHP200491	Start Date*: 2021-08-03
Sponsor Name:Assistance Publique – Hôpitaux de Paris
Full Title: Impact of post-ARDS COVID sedation on late neuroinflammation
Medical condition: All patients who have developed and survived ARDS linked to COVID-19 infection, admitted to intensive care units, meeting the study's inclusion criteria may be included in this research.
Disease:
Population Age: Adults, Elderly		Gender: Male, Female
Trial protocol: FR (Trial now transitioned)
Trial results: (No results available)

EudraCT Number: 2019-003581-41	Sponsor Protocol Number: J2J-MC-JZLA	Start Date*: 2020-09-08
Sponsor Name:Eli Lilly and Company
Full Title: EMBER: A Phase 1a/1b Study of LY3484356 Administered as Monotherapy and in Combination with Anticancer Therapies for Patients with ER+ Locally Advanced or Metastatic Breast Cancer and Other Select ...
Medical condition: ER+ Locally Advanced or Metastatic Breast Cancer and Other Select Non-Breast Cancers
Disease:
Population Age: Adults, Elderly		Gender: Male, Female
Trial protocol: FR (Trial now transitioned) BE (Trial now transitioned)
Trial results: (No results available)

EudraCT Number: 2021-002308-11

Sponsor Protocol Number: IM047-001

Start Date*: 2021-12-22

Sponsor Name:Celgene International II Sàrl

Full Title: A phase 2/3, multicenter, randomized, double-blind study to evaluate the efficacy, safety, pharmacokinetics and pharmacodynamics of oral ozanimod (RPC1063) in pediatric subjects with moderately to ...

Medical condition: Moderately to Severely Active Ulcerative Colitis

Disease:	Version	SOC Term	Classification Code	Term	Level
Disease:	20.1	100000004856	10045365	Ulcerative colitis	LLT

Population Age: Children, Adolescents, Under 18

Gender: Male, Female

Trial protocol: FR (Trial now transitioned) PL (Trial now transitioned) DE (Trial now transitioned) ES (Ongoing) BE (Trial now transitioned)

Trial results: (No results available)

EudraCT Number: 2020-000309-10

Sponsor Protocol Number: CHUBX2017/45

Start Date*: 2021-10-04

Sponsor Name:CHU de Bordeaux

Full Title: Phase II/III double-blind randomized placebo-controlled trial assessing the preventive effect of Clopidogrel on the systemic sclerosis development risk in subjects with specific dysimmunity and Ray...

Medical condition: Raynaud phenomenon

Disease:	Version	SOC Term	Classification Code	Term	Level
Disease:	20.0	100000004866	10037914	Raynaud's syndrome	LLT

Population Age: Adults, Elderly

Gender: Male, Female

Trial protocol: FR (Trial now transitioned)

Trial results: (No results available)

EudraCT Number: 2020-005896-12

Sponsor Protocol Number: CBYL719F12401

Start Date*: 2021-10-20

Sponsor Name:Novartis Pharma AG

Full Title: EPIK-P3: A phase II study to evaluate the long-term safety and efficacy of alpelisib in patients with PIK3CA-Related Overgrowth Spectrum (PROS) who previously participated in Study CBYL719F12002 (E...

Medical condition: PIK3CA-related overgrowth spectrum (PROS)

Disease:	Version	SOC Term	Classification Code	Term	Level
Disease:	21.1	10010331 - Congenital, familial and genetic disorders	10081236	PIK3CA related overgrowth spectrum	PT

Population Age: Children, Adolescents, Under 18, Adults

Gender: Male, Female

Trial protocol: FR (Trial now transitioned) IE (Trial now transitioned) ES (Ongoing)

Trial results: (No results available)

EudraCT Number: 2021-003478-30

Sponsor Protocol Number: CAAA802A12101

Start Date*: 2022-08-15

Sponsor Name:Novartis Pharma AG

Full Title: SatisfACtion: A Phase I/II, open-label, multi-center study of [225Ac]Ac-PSMA-R2 in men with heavily pre-treated PSMA-positive metastatic castration-resistant prostate cancer (mCRPC) with or without...

Medical condition: PSMA-positive Metastatic Castration-resistant Prostate Cancer (mCRPC) with or without prior 177Lu-PSMA radioligand therapy.

Disease:	Version	SOC Term	Classification Code	Term	Level
Disease:	20.0	100000004864	10036908	Prostatic neoplasms malignant	HLT

Population Age: Adults, Elderly

Gender: Male

Trial protocol: FR (Trial now transitioned)

Trial results: (No results available)

EudraCT Number: 2021-000161-32	Sponsor Protocol Number: CLIN-52120-452	Start Date*: 2021-08-11
Sponsor Name:Ipsen Pharma
Full Title: A Multicentre, Interventional, Post-marketing, Randomised, Double-blind, Crossover Study to Evaluate the Clinical Safety and Efficacy of AbobotulinumtoxinA (Dysport®) in Comparison with Onabotulinu...
Medical condition: upper limb spasticity (ULS) of any aetiology (in US and France) or post-stroke ULS (in Canada)
Disease:
Population Age: Adults, Elderly		Gender: Male, Female
Trial protocol: FR (Trial now transitioned)
Trial results: (No results available)

EudraCT Number: 2018-004124-10

Sponsor Protocol Number: 68284528MMY2003

Start Date*: 2020-08-07

Sponsor Name:Janssen-Cilag International NV

Full Title: A Phase 2, Multicohort Open-Label Study of JNJ-68284528, a Chimeric Antigen Receptor T cell (CAR-T) Therapy Directed Against BCMA in Subjects with Multiple Myeloma

Medical condition: Multiple Myeloma

Disease:	Version	SOC Term	Classification Code	Term	Level
Disease:	21.0	100000004864	10028228	Multiple myeloma	LLT

Population Age: Adults, Elderly

Gender: Male, Female

Trial protocol: FR (Trial now transitioned) DE (Trial now transitioned) BE (Trial now transitioned) ES (Ongoing) NL (Trial now transitioned)

Trial results: (No results available)

EudraCT Number: 2014-001578-32	Sponsor Protocol Number: 2012/49	Start Date*: 2014-11-10
Sponsor Name:CENTRE ANTOINE LACASSAGNE
Full Title: A phase I/II study of pazopanib in combination with temozolomide in patients with newly diagnosed glioblastoma multiforme after surgery and RT-CT (PAZOGLIO study)
Medical condition: Glioblastoma
Disease:
Population Age: Adults, Elderly		Gender: Male, Female
Trial protocol: FR (Trial now transitioned)
Trial results: (No results available)

EudraCT Number: 2017-002400-26

Sponsor Protocol Number: 64407564MMY1001

Start Date*: 2019-02-06

Sponsor Name:Janssen-Cilag International NV

Full Title: A Phase 1/2, First-in-Human, Open-Label, Dose Escalation Study of Talquetamab, a Humanized GPRC5D x CD3 Bispecific Antibody, in Subjects with Relapsed or Refractory Multiple Myeloma

Medical condition: Relapsed or Refractory Multiple Myeloma

Disease:	Version	SOC Term	Classification Code	Term	Level
Disease:	20.0	10010331 - Congenital, familial and genetic disorders	10005330	Blood and lymphatic system disorders congenital	HLGT

Population Age: Adults, Elderly

Gender: Male, Female

Trial protocol: NL (Trial now transitioned) DE (Trial now transitioned) PL (Trial now transitioned) FR (Trial now transitioned) BE (Trial now transitioned)

Trial results: (No results available)

EudraCT Number: 2020-001685-11	Sponsor Protocol Number: ICO-2020-01	Start Date*: 2020-06-26
Sponsor Name:INSTITUT DE CANCEROLOGIE DE L'OUEST
Full Title: RElapse in previously irradiated Prostate bed : a phase I/II study of stereotactic Ablative reIRradiation potentiated by Metformine
Medical condition: RElapse in previously irradiated Prostate bed
Disease:
Population Age: Adults		Gender: Male
Trial protocol: FR (Trial now transitioned)
Trial results: (No results available)

EudraCT Number: 2019-003047-30

Sponsor Protocol Number: 209664

Start Date*: 2020-02-14

Sponsor Name:GlaxoSmithKline Research & Development Ltd

Full Title: A Phase 3, Randomized, Open-Label Study of Belantamab Mafodotin Administered in Combination with Bortezomib, Lenalidomide and Dexamethasone Versus Bortezomib, Lenalidomide and Dexamethasone Alone i...

Medical condition: Multiple Myeloma

Disease:	Version	SOC Term	Classification Code	Term	Level
Disease:	21.0	100000004864	10028228	Multiple myeloma	LLT

Population Age: Adults, Elderly

Gender: Male, Female

Trial protocol: FR (Trial now transitioned)

Trial results: (No results available)

EudraCT Number: 2018-000186-36

Sponsor Protocol Number: IB2017-04

Start Date*: 2019-01-07

Sponsor Name:Institut Bergonié

Full Title: Phase III trial investigating the potential benefit of intensified peri-operative Chemotherapy in patients with in high-risk CINSARC patients with resectable soft-tissue SARComas

Medical condition: Resectable, non-metastatic soft-tissue sarcoma (STS)

Disease:	Version	SOC Term	Classification Code	Term	Level
Disease:	20.0	100000004864	10039494	Sarcoma NOS	LLT

Population Age: Adults, Elderly

Gender: Male, Female

Trial protocol: FR (Trial now transitioned)

Trial results: (No results available)

EudraCT Number: 2007-007616-28

Sponsor Protocol Number: RV-MM-PI-302

Start Date*: 2008-01-31

Sponsor Name:FONDAZIONE NEOPLASIE SANGUE ONLUS

Full Title: A MULTICENTER, OPEN LABEL STUDY OF ORAL REVLIMID AND PREDNISONE (RP) FOLLOWED BY ORAL REVLIMID MELPHALAN AND PREDNISONE (MPR) IN NEWLY DIAGNOSED ELDERLY MULTIPLE MYELOMA PATIENTS

Medical condition: NEWLY DIAGNOSED ELDERLY MULTIPLE MYELOMA PATIENTS

Disease:	Version	SOC Term	Classification Code	Term	Level
Disease:	9.1		10028229	Multiple myelomas	HLT

Population Age: Elderly

Gender: Male, Female

Trial protocol: IT (Completed)

Trial results: View results

EudraCT Number: 2017-000087-15

Sponsor Protocol Number: BP39529

Start Date*: 2017-12-21

Sponsor Name:F. Hoffmann-La Roche Ltd

Full Title: A RANDOMIZED, DOUBLE-BLIND, PLACEBOCONTROLLED, 52-WEEK PHASE II STUDY TO EVALUATE THE EFFICACY OF INTRAVENOUS RO7046015/PRASINEZUMAB (PRX002) IN PARTICIPANTS WITH EARLY PARKINSON'S DISEASE WITH A 6...

Medical condition: Parkinson’s disease

Disease:	Version	SOC Term	Classification Code	Term	Level
Disease:	20.0	10029205 - Nervous system disorders	10061536	Parkinson's disease	PT

Population Age: Adults, Elderly

Gender: Male, Female

Trial protocol: DE (Trial now transitioned) AT (Trial now transitioned) ES (Ongoing) FR (Trial now transitioned)

Trial results: View results

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The status and protocol content of GB trials is no longer updated since 1 January 2021. For the UK, as of 31 January 2021, EU Law applies only to the territory of Northern Ireland (NI) to the extent foreseen in the Protocol on Ireland/NI. Legal notice
As of 31 January 2023, all EU/EEA initial clinical trial applications must be submitted through CTIS . Updated EudraCT trials information and information on PIP/Art 46 trials conducted exclusively in third countries continues to be submitted through EudraCT and published on this website.

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