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    Summary
    EudraCT Number:2015-001600-64
    Sponsor's Protocol Code Number:RPC01-3102
    National Competent Authority:Germany - BfArM
    Clinical Trial Type:EEA CTA
    Trial Status:Completed
    Date on which this record was first entered in the EudraCT database:2015-08-04
    Trial results
    Index
    A. PROTOCOL INFORMATION
    B. SPONSOR INFORMATION
    C. APPLICANT IDENTIFICATION
    D. IMP IDENTIFICATION
    D.8 INFORMATION ON PLACEBO
    E. GENERAL INFORMATION ON THE TRIAL
    F. POPULATION OF TRIAL SUBJECTS
    G. INVESTIGATOR NETWORKS TO BE INVOLVED IN THE TRIAL
    N. REVIEW BY THE COMPETENT AUTHORITY OR ETHICS COMMITTEE IN THE COUNTRY CONCERNED
    P. END OF TRIAL
    Expand All   Collapse All
    A. Protocol Information
    A.1Member State ConcernedGermany - BfArM
    A.2EudraCT number2015-001600-64
    A.3Full title of the trial
    A Phase 3, Multicenter, Open-Label Extension Trial of Oral RPC1063 as Therapy for Moderate to Severe Ulcerative Colitis
    A.3.1Title of the trial for lay people, in easily understood, i.e. non-technical, language
    The purpose of this study is to determine whether long-term RPC1063 is safe and effective in the treatment of ulcerative colitis (UC).
    A.3.2Name or abbreviated title of the trial where available
    Efficacy and Safety Study of long-term RPC1063 in Ulcerative Colitis
    A.4.1Sponsor's protocol code numberRPC01-3102
    A.5.2US NCT (ClinicalTrials.gov registry) numberNCT02531126
    A.7Trial is part of a Paediatric Investigation Plan No
    A.8EMA Decision number of Paediatric Investigation Plan
    B. Sponsor Information
    B.Sponsor: 1
    B.1.1Name of SponsorCelgene International II Sàrl (CIS II)
    B.1.3.4CountrySwitzerland
    B.3.1 and B.3.2Status of the sponsorCommercial
    B.4 Source(s) of Monetary or Material Support for the clinical trial:
    B.4.1Name of organisation providing supportCelgene International II Sàrl (CIS II)
    B.4.2CountrySwitzerland
    B.5 Contact point designated by the sponsor for further information on the trial
    B.5.1Name of organisationCelgene International II Sarl
    B.5.2Functional name of contact pointTruenorth Study Information Center
    B.5.3 Address:
    B.5.3.1Street Address3033 Science Park Road, Suite 300
    B.5.3.2Town/ citySan Diego, California
    B.5.3.3Post code92121
    B.5.3.4CountryUnited States
    B.5.4Telephone number+18442669299
    B.5.6E-mailtruenorth@quintiles.com
    D. IMP Identification
    D.IMP: 1
    D.1.2 and D.1.3IMP RoleTest
    D.2 Status of the IMP to be used in the clinical trial
    D.2.1IMP to be used in the trial has a marketing authorisation Yes
    D.2.1.1.1Trade name ZEPOSIA® (ozanimod)
    D.2.1.1.2Name of the Marketing Authorisation holderCelegene Corporation
    D.2.1.2Country which granted the Marketing AuthorisationUnited States
    D.2.5The IMP has been designated in this indication as an orphan drug in the Community No
    D.2.5.1Orphan drug designation number
    D.3 Description of the IMP
    D.3.1Product name0.25 mg RPC1063
    D.3.2Product code RPC1063
    D.3.4Pharmaceutical form Capsule, hard
    D.3.4.1Specific paediatric formulation No
    D.3.7Routes of administration for this IMPOral use
    D.3.8 to D.3.10 IMP Identification Details (Active Substances)
    D.3.8INN - Proposed INNOzanimod
    D.3.9.2Current sponsor codeRPC1063
    D.3.9.3Other descriptive name(S)-5-(3-(1-((2-hydroxyethyl)amino)-2,3-dihydro-1H-inden-4-yl)-1,2,4-oxadiazol-5-yl)-2-isopropoxybenzonitrile hydrochloride
    D.3.9.4EV Substance CodeSUB175614
    D.3.10 Strength
    D.3.10.1Concentration unit mg milligram(s)
    D.3.10.2Concentration typeequal
    D.3.10.3Concentration number0.25
    D.3.11 The IMP contains an:
    D.3.11.1Active substance of chemical origin Yes
    D.3.11.2Active substance of biological/ biotechnological origin (other than Advanced Therapy IMP (ATIMP) No
    The IMP is a:
    D.3.11.3Advanced Therapy IMP (ATIMP) No
    D.3.11.3.1Somatic cell therapy medicinal product No
    D.3.11.3.2Gene therapy medical product No
    D.3.11.3.3Tissue Engineered Product No
    D.3.11.3.4Combination ATIMP (i.e. one involving a medical device) No
    D.3.11.3.5Committee on Advanced therapies (CAT) has issued a classification for this product No
    D.3.11.4Combination product that includes a device, but does not involve an Advanced Therapy No
    D.3.11.5Radiopharmaceutical medicinal product No
    D.3.11.6Immunological medicinal product (such as vaccine, allergen, immune serum) No
    D.3.11.7Plasma derived medicinal product No
    D.3.11.8Extractive medicinal product No
    D.3.11.9Recombinant medicinal product No
    D.3.11.10Medicinal product containing genetically modified organisms No
    D.3.11.11Herbal medicinal product No
    D.3.11.12Homeopathic medicinal product No
    D.3.11.13Another type of medicinal product No
    D.IMP: 2
    D.1.2 and D.1.3IMP RoleTest
    D.2 Status of the IMP to be used in the clinical trial
    D.2.1IMP to be used in the trial has a marketing authorisation Yes
    D.2.1.1.1Trade name ZEPOSIA® (ozanimod)
    D.2.1.1.2Name of the Marketing Authorisation holderCelegene Corporation
    D.2.1.2Country which granted the Marketing AuthorisationUnited States
    D.2.5The IMP has been designated in this indication as an orphan drug in the Community No
    D.2.5.1Orphan drug designation number
    D.3 Description of the IMP
    D.3.1Product name1.0 mg RPC1063
    D.3.2Product code RPC1063
    D.3.4Pharmaceutical form Capsule, hard
    D.3.4.1Specific paediatric formulation No
    D.3.7Routes of administration for this IMPOral use
    D.3.8 to D.3.10 IMP Identification Details (Active Substances)
    D.3.8INN - Proposed INNOzanimod
    D.3.9.2Current sponsor codeRPC1063
    D.3.9.3Other descriptive name(S)-5-(3-(1-((2-hydroxyethyl)amino)-2,3-dihydro-1H-inden-4-yl)-1,2,4-oxadiazol-5-yl)-2-isopropoxybenzonitrile hydrochloride
    D.3.9.4EV Substance CodeSUB175614
    D.3.10 Strength
    D.3.10.1Concentration unit mg milligram(s)
    D.3.10.2Concentration typeequal
    D.3.10.3Concentration number1.0
    D.3.11 The IMP contains an:
    D.3.11.1Active substance of chemical origin Yes
    D.3.11.2Active substance of biological/ biotechnological origin (other than Advanced Therapy IMP (ATIMP) No
    The IMP is a:
    D.3.11.3Advanced Therapy IMP (ATIMP) No
    D.3.11.3.1Somatic cell therapy medicinal product No
    D.3.11.3.2Gene therapy medical product No
    D.3.11.3.3Tissue Engineered Product No
    D.3.11.3.4Combination ATIMP (i.e. one involving a medical device) No
    D.3.11.3.5Committee on Advanced therapies (CAT) has issued a classification for this product No
    D.3.11.4Combination product that includes a device, but does not involve an Advanced Therapy No
    D.3.11.5Radiopharmaceutical medicinal product No
    D.3.11.6Immunological medicinal product (such as vaccine, allergen, immune serum) No
    D.3.11.7Plasma derived medicinal product No
    D.3.11.8Extractive medicinal product No
    D.3.11.9Recombinant medicinal product No
    D.3.11.10Medicinal product containing genetically modified organisms No
    D.3.11.11Herbal medicinal product No
    D.3.11.12Homeopathic medicinal product No
    D.3.11.13Another type of medicinal product No
    D.8 Information on Placebo
    E. General Information on the Trial
    E.1 Medical condition or disease under investigation
    E.1.1Medical condition(s) being investigated
    Ulcerative colitis
    E.1.1.1Medical condition in easily understood language
    ulcerative colitis
    E.1.1.2Therapeutic area Diseases [C] - Digestive System Diseases [C06]
    MedDRA Classification
    E.1.2 Medical condition or disease under investigation
    E.1.2Version 20.1
    E.1.2Level LLT
    E.1.2Classification code 10045365
    E.1.2Term Ulcerative colitis
    E.1.2System Organ Class 100000004856
    E.1.3Condition being studied is a rare disease No
    E.2 Objective of the trial
    E.2.1Main objective of the trial
    Evaluate the long-term safety of RPC1063 for the treatment of all patients with moderate to severe UC.
    Evaluate the long-term safety of RPC1063 for the treatment of adult patients with moderate to severe UC.
    E.2.2Secondary objectives of the trial
    Not applicable
    E.2.3Trial contains a sub-study No
    E.3Principal inclusion criteria
    1. Previously participated in a trial of RPC1063 (eg, RPC01-3101 or
    completed at least 1 year of the open-label period of RPC01-202) and
    meet the criteria for participation in the open label extension as outlined in the prior trial
    2. Females patients of childbearing potential (FCBP)*:
    Must agree to practice a highly effective method of contraception**
    throughout the trial until completion of the 90-day Safety Follow-up
    Visit. Highly effective methods of contraception are those that alone or in combination result in a failure rate of a Pearl index of less than 1% per year when used consistently and correctly. Acceptable methods of birth control in the trial are the following:
    -combined hormonal (oestrogen and progestogen containing)
    contraception, which may be oral, intravaginal, or transdermal
    -progestogen-only hormonal contraception associated with inhibition of ovulation, which may be oral, injectable, or implantable
    -placement of an intrauterine device (IUD)
    -placement of an intrauterine hormone-releasing system (IUS)
    -bilateral tubal occlusion
    -vasectomized partner
    -complete sexual abstinence
    *For the purposes of this study, a female patient is considered to be of childbearing potential if she has reached menarche, and 1) has not undergone a hysterectomy (the surgical removal of the uterus) or bilateral oophorectomy (the surgical removal of both ovaries) or 2) has not been postmeopausal for at least 24 consecutive months (that is, has had menses at any time during the preceding 24 consecutive months)
    **Contaception Education: Counselling about pregnancy prcautions and the potential risks of fetal exposure must be conducted for FCBP. The Investigator will educate all FCBP about the different options of contraceptive methods or abstinence, as appropriate, at the Screening and Basline Visits. The patient will be re-educated every time her contrceptive measures/methods or ability to become pregnant changes. The female patient's chosen form of contraception must be effective by the time the femal patient is randomized into the study (for example, hormonal contraception should be initiated at least 28 days before baseline).
    Periodic abstinence (calendar, symptothermal, post-ovulaiton methods), withdrawal (coitus interruptus), spermicides only, and lactational amenorrhea method are not acceptable methods of contraception.
    3. Must provide written informed consent and have the ability to be compliant with the schedule of protocol assessments, which must be
    obtained prior to any trial-related procedures.
    E.4Principal exclusion criteria
    Exclusions Related to Medications:
    1. Have received any of the following therapies since the first dose of
    investigational drug in the prior RPC1063 trial:
    • Treatment with a biologic agent
    • Treatment with an investigational agent other than RPC1063
    • Treatment with D-penicillamine, leflunomide, thalidomide, natalizumab, fingolimod, etrasimod, or tofacitinib
    • Treatment with lymphocyte-depleting therapies (e.g., Campath, anti- CD4, cladribine, rituximab, ocrelizumab, cyclophosphamide,
    mitoxantrone, total body irradiation, bone marrow transplantation,
    alemtuzumab, daclizumab)
    • Treatment with a live vaccine or live attenuated vaccine within 4
    weeks prior to Visit 1 of this trial
    2. Are currently receiving or require initiation of any of the following
    therapies:
    • Treatment with corticosteroids at a dose that exceeds the prednisone equivalent of >40 mg
    • Treatment with immunosuppressive agents (e.g., azathioprine, 6-MP, or methotrexate)
    • Chronic non-steroidal anti-inflammatory drug (NSAID) use (Note:
    occasional use of NSAIDs and acetaminophen [eg, headache, arthritis,
    myalgias, or menstrual cramps] and aspirin up to 325 mg/day is
    permitted)
    • Treatment with Class Ia or Class III anti-arrhythmic drugs or
    treatment with two or more agents in combination known to prolong PR interval
    3. Are receiving treatment with any of the following drugs or
    interventions within the corresponding timeframe:
    At Day 1
    - CYP2C8 inhibitors (eg, gemfibrozil or clopidogrel) or inducers (eg,
    rifampicin)
    • Two weeks prior to Day 1
    - Monoamine oxidase inhibitors (eg, selegiline, phenelzine)
    4. Are receiving treatment with breast cancer resistance protein (BCRP) inhibitors (eg, cyclosporine, eltrombopag)
    Exclusions Related to General Health:
    5. Pregnancy, lactation, or a positive serum beta human chorionic
    gonadotropin (hCG)
    6. Clinically relevant hepatic, neurological, pulmonary, ophthalmological, endocrine, psychiatric or other major systemic disease making implementation of the protocol or interpretation of the trial difficult or that would put the patient at risk by participating in the trial or that would have required a patient to discontinue treatment in previous RPC1063 trial
    7. Clinically relevant cardiovascular conditions, including history or
    presence of recent myocardial infarction, unstable angina, stroke,
    transient ischemic attack; decompensated heart failure requiring
    hospitalization, Class III/IV heart failure, sick sinus syndrome, or severe untreated sleep apnea
    Exclusions Related to Laboratory Results:
    8. Liver function impairment or persisting elevations of aspartate
    aminotransferase (AST) or alanine aminotransferase (ALT) > 5 times the
    upper limit of normal (ULN), or direct bilirubin > 3 times the ULN
    9. FEV1 or FVC < 50% of predicted values
    E.5 End points
    E.5.1Primary end point(s)
    Due to the open-label nature of the trial and the lack of a control group, all data will be summarized and no hypothesis testing will be performed. Each efficacy endpoint will be summarized and 95% confidence intervals around the estimates may also be presented.

    Efficacy Endpoints:
    • Proportion of patients in clinical remission.
    • Proportion of patients with a clinical response
    • Proportion of patients with endoscopic improvement
    • Proportion of patients with mucosal healing
    • Proportion of patients with corticosteroid-free remission
    • Change from Baseline in complete Mayo score, partial Mayo score, and
    9-point Mayo score
    • Proportion of patients with histologic remission
    • Proportion of patients with clinical response, clinical remission, or endoscopic improvement in patients who had previously received anti-TNF therapy

    Safety Endpoints:
    The incidence, severity, and relationship of treatment-emergent adverse
    events (TEAEs), serious AEs (SAEs), TEAEs leading to discontinuation of
    investigational drug, and TEAEs of special interest will be summarized,
    - Exploratory safety endpoints include changes from baseline for clinical
    laboratory measures, vital signs, ECGs, and pulmonary function tests.

    Other Exploratory Endpoints:
    Absolute lymphocyte count (ALC) derived from hematology laboratory results
    Plasma protein biomarkers (cytokines, chemokines, other markers of inflammation)
    - Stool biomarkers (eg FCP)
    - Mucosal tissue inflammatory biomarkers (eg, lymphocyte subsets)
    - Exploratory measurements of immune response (e.g. SARS-CoV-2
    serology), from blood samples collected after the amendment, every 6
    months thereafter and end of treatment, and the potential association
    between these measurements and selected endpoints related to safety,
    efficacy, and/or biomarkers.
    E.5.1.1Timepoint(s) of evaluation of this end point
    Efficacy assessments will be performed at the following visits;
    Day 1 (Baseline/Visit 1) - All
    Week 5 (Visit 2)
    Week 10 (Visit 3)
    Week 16 (Visit 4)
    Week 22 (Visit 5)
    Week34 (Visit 6)
    Week 46 (visit 7)
    Thereafter, additional visits at 24-week intervals (Visit 8 onwards).

    Partial Mayo partial score assessment to be performed at each visit.
    Full Mayo score assessment performed at Visit 1, Visit 7, and after that, at 48-week intervals (i.e.. Week 94, Week 142, etc.) and at the End of Treatment/Early Termination Visit.

    Endoscopy and colonic biopsies will be performed at Week 1, Visit 7, and after that, at 48-week intervals (i.e.. Week 94, Week 142, etc.) and at the End of Treatment/Early Termination Visit.
    E.5.2Secondary end point(s)
    Not applicable
    E.5.2.1Timepoint(s) of evaluation of this end point
    Not applicable
    E.6 and E.7 Scope of the trial
    E.6Scope of the trial
    E.6.1Diagnosis No
    E.6.2Prophylaxis No
    E.6.3Therapy Yes
    E.6.4Safety Yes
    E.6.5Efficacy Yes
    E.6.6Pharmacokinetic Yes
    E.6.7Pharmacodynamic Yes
    E.6.8Bioequivalence No
    E.6.9Dose response No
    E.6.10Pharmacogenetic No
    E.6.11Pharmacogenomic No
    E.6.12Pharmacoeconomic No
    E.6.13Others No
    E.7Trial type and phase
    E.7.1Human pharmacology (Phase I) No
    E.7.1.1First administration to humans No
    E.7.1.2Bioequivalence study No
    E.7.1.3Other No
    E.7.1.3.1Other trial type description
    E.7.2Therapeutic exploratory (Phase II) No
    E.7.3Therapeutic confirmatory (Phase III) Yes
    E.7.4Therapeutic use (Phase IV) No
    E.8 Design of the trial
    E.8.1Controlled No
    E.8.1.1Randomised No
    E.8.1.2Open Yes
    E.8.1.3Single blind No
    E.8.1.4Double blind No
    E.8.1.5Parallel group No
    E.8.1.6Cross over No
    E.8.1.7Other No
    E.8.2 Comparator of controlled trial
    E.8.2.1Other medicinal product(s) No
    E.8.2.2Placebo No
    E.8.2.3Other No
    E.8.3 The trial involves single site in the Member State concerned No
    E.8.4 The trial involves multiple sites in the Member State concerned Yes
    E.8.4.1Number of sites anticipated in Member State concerned12
    E.8.5The trial involves multiple Member States Yes
    E.8.5.1Number of sites anticipated in the EEA93
    E.8.6 Trial involving sites outside the EEA
    E.8.6.1Trial being conducted both within and outside the EEA Yes
    E.8.6.2Trial being conducted completely outside of the EEA No
    E.8.6.3If E.8.6.1 or E.8.6.2 are Yes, specify the regions in which trial sites are planned
    Argentina
    Australia
    Belarus
    Belgium
    Bulgaria
    Canada
    Czechia
    Germany
    Hungary
    Israel
    Italy
    Korea, Republic of
    Netherlands
    New Zealand
    Poland
    Russian Federation
    Slovakia
    South Africa
    Ukraine
    United Kingdom
    United States
    E.8.7Trial has a data monitoring committee Yes
    E.8.8 Definition of the end of the trial and justification where it is not the last visit of the last subject undergoing the trial
    Patients will receive treatment until the end of March 2023, unless the Sponsor discontinues the development program.
    E.8.9 Initial estimate of the duration of the trial
    E.8.9.1In the Member State concerned years7
    E.8.9.1In the Member State concerned months6
    E.8.9.1In the Member State concerned days24
    E.8.9.2In all countries concerned by the trial years7
    E.8.9.2In all countries concerned by the trial months6
    E.8.9.2In all countries concerned by the trial days24
    F. Population of Trial Subjects
    F.1 Age Range
    F.1.1Trial has subjects under 18 No
    F.1.1.1In Utero No
    F.1.1.2Preterm newborn infants (up to gestational age < 37 weeks) No
    F.1.1.3Newborns (0-27 days) No
    F.1.1.4Infants and toddlers (28 days-23 months) No
    F.1.1.5Children (2-11years) No
    F.1.1.6Adolescents (12-17 years) No
    F.1.2Adults (18-64 years) Yes
    F.1.2.1Number of subjects for this age range: 1164
    F.1.3Elderly (>=65 years) Yes
    F.1.3.1Number of subjects for this age range: 36
    F.2 Gender
    F.2.1Female Yes
    F.2.2Male Yes
    F.3 Group of trial subjects
    F.3.1Healthy volunteers No
    F.3.2Patients Yes
    F.3.3Specific vulnerable populations Yes
    F.3.3.1Women of childbearing potential not using contraception No
    F.3.3.2Women of child-bearing potential using contraception Yes
    F.3.3.3Pregnant women No
    F.3.3.4Nursing women No
    F.3.3.5Emergency situation No
    F.3.3.6Subjects incapable of giving consent personally No
    F.3.3.7Others No
    F.4 Planned number of subjects to be included
    F.4.1In the member state53
    F.4.2 For a multinational trial
    F.4.2.1In the EEA 614
    F.4.2.2In the whole clinical trial 1350
    F.5 Plans for treatment or care after the subject has ended the participation in the trial (if it is different from the expected normal treatment of that condition)
    Patients who leave the trial and complete their end of trial assessments, including the Safety Follow-up Visit do not require any additional care provided by the sponsor; they will return to the care of their personal physician(s).
    G. Investigator Networks to be involved in the Trial
    N. Review by the Competent Authority or Ethics Committee in the country concerned
    N.Competent Authority Decision Authorised
    N.Date of Competent Authority Decision2015-09-23
    N.Ethics Committee Opinion of the trial applicationFavourable
    N.Ethics Committee Opinion: Reason(s) for unfavourable opinion
    N.Date of Ethics Committee Opinion2015-11-13
    P. End of Trial
    P.End of Trial StatusCompleted
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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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