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Clinical trials for Ketotifen

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   44334   clinical trials with a EudraCT protocol, of which   7366   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 ).  
     
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    7 result(s) found for: Ketotifen. Displaying page 1 of 1.
    EudraCT Number: 2022-002311-39 Sponsor Protocol Number: 101069207 Start Date*: 2022-09-07
    Sponsor Name:University Of Cyprus
    Full Title: Phase II trial for the use of ketotifen to enhance therapy in patients with sarcoma receiving standard chemotherapy
    Medical condition: Patients with sarcoma
    Disease:
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: CY (Completed)
    Trial results: (No results available)
    EudraCT Number: 2005-003381-41 Sponsor Protocol Number: PS-W07 Start Date*: 2006-04-25
    Sponsor Name:Pharma Stulln GmbH
    Full Title: Innerhalb der Strata randomisierte, kontrollierte, für den Prüfarzt verblindete klinische Prüfung zur Untersuchung der Wirksamkeit von Keto-Stulln® UD im Vergleich zu Zaditen® ophtha sine am Auge i...
    Medical condition: Symptomatische Behandlung einer jahreszeitlich bedingten allergischen Conjunctivitis
    Disease:
    Population Age: Adults Gender: Male, Female
    Trial protocol: DE (Completed)
    Trial results: View results
    EudraCT Number: 2006-005681-39 Sponsor Protocol Number: FAR-0201 Start Date*: 2007-01-22
    Sponsor Name:FARMIGEA
    Full Title: A RANDOMIZED, DOUBLE-BLIND, MULTICENTER PARALLEL GROUP STUDY ON EFFICACY AND SAFETY OF KETOTIFEN FUMARATE 0.05 OPHTHALMIC SOLUTION VERSUS KETOTIFEN FUMARATE 0.025
    Medical condition: Patients with seasonal allergic conjunctivitis and history of ocular allergies for at least 2 years.
    Disease: Version SOC Term Classification Code Term Level
    6.1 10010744 PT
    Population Age: Adolescents, Under 18, Adults, Elderly Gender: Male, Female
    Trial protocol: IT (Completed)
    Trial results: (No results available)
    EudraCT Number: 2006-003689-32 Sponsor Protocol Number: FARM5YZTZW Start Date*: 2006-12-19
    Sponsor Name:UNIVERSITA CAMPUS BIOMEDICO
    Full Title: Multicenter, randomised, double masked, controlled studies on the efficacy of Cyclosporine eye drop treatment in preventing Vernal Keratoconjunctivitis VKC relapses and in treating the acute phase.
    Medical condition: VERNAL KERATOCONJUNTIVITIS
    Disease: Version SOC Term Classification Code Term Level
    9.1 10021877 Ocular infections, irritations and inflammations HLGT
    Population Age: Children, Adolescents, Under 18 Gender: Male, Female
    Trial protocol: IT (Completed)
    Trial results: (No results available)
    EudraCT Number: 2005-002748-24 Sponsor Protocol Number: PS-V06 Start Date*: Information not available in EudraCT
    Sponsor Name:Pharma Stulln GmbH
    Full Title: Randomisierte, kontrollierte, doppelblinde klinische Prüfung zur Untersuchung der Verträglichkeit von Keto-Stulln® UD im Vergleich zu physiologischer Kochsalzlösung am Auge in einem intraindividuel...
    Medical condition: Gesunde Probanden.
    Disease:
    Population Age: Children, Adolescents, Under 18, Adults Gender: Male, Female
    Trial protocol: DE (Completed)
    Trial results: View results
    EudraCT Number: 2009-018155-16 Sponsor Protocol Number: STA-ALUMITES-2010-01 Start Date*: 2010-11-25
    Sponsor Name:STALLERGENES IBÉRICA S.A.
    Full Title: Estudio multicéntrico, aleatorizado, abierto, para evaluar la eficacia del tratamiento con inmunoterapia subcutánea con ácaros (Alustal Rapid) mediante rinometría acústica tras provocación nasal en...
    Medical condition: Rinitis Alérgica
    Disease: Version SOC Term Classification Code Term Level
    11 10001723 Rinitis alérgica LLT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: ES (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2007-000130-39 Sponsor Protocol Number: NEO014/FP/pMDI/paed Start Date*: 2007-02-08
    Sponsor Name:Neolab Ltd
    Full Title: A PHASE III, RANDOMISED, DOUBLE-BLIND, DOUBLE-DUMMY, PLACEBO CONTROLLED CROSSOVER STUDY TO COMPARE THE SYSTEMIC EFFECTS OF INHALED FLUTICASONE PROPIONATE HFA MDI 200g PER DAY VERSUS THE REFERENCE ...
    Medical condition: Mild asthma in pre-pubertal children.
    Disease: Version SOC Term Classification Code Term Level
    9.1 10003553 Asthma LLT
    Population Age: Children, Under 18 Gender: Male, Female
    Trial protocol: DK (Completed)
    Trial results: (No results available)
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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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