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Durvalumab Plus Olaparib Administered Prior to Surgery of Resectable Urothelial Bladder Cancer (NEODURVARIB) (NEODURVARIB)

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ClinicalTrials.gov Identifier: NCT03534492
Recruitment Status : Not yet recruiting
First Posted : May 23, 2018
Last Update Posted : May 25, 2018
Sponsor:
Collaborators:
AstraZeneca
Sistemas Genómicos
Apices Soluciones S.L.
Information provided by (Responsible Party):
Spanish Oncology Genito-Urinary Group

Brief Summary:
The standard of care for muscle-invasive bladder cancer (MIBC) is radical cystectomy, which is rarely curative. Platinum-based neoadjuvant chemotherapy is associated with an improvement in Overall Survival (OS), but only a few patients can benefit from this approach. Therefore, new neoadjuvant treatments are required for muscle- invasive bladder cancer. In this study it will be explored the activity of durvalumab plus olaparib in advanced Transitional Cell Carcinoma of the Bladder and therefore may have beneficial outcomes in the neoadjuvant setting. Adverse events associated with durvalumab and olaparib is one of the potential risks in this study. Participation in this trial, in which 6-8 weeks of preoperative treatment will be administered, is not expected to result in delays of surgery for participants. It is not foreseen that treatment with durvalumab and olaparib has a relevant impact on operability or increases the risks associated with surgery

Condition or disease Intervention/treatment Phase
Bladder Cancer Drug: Durvalumab Drug: Olaparib Phase 2

Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 29 participants
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Impact of the Combination of Durvalumab (MEDI4736) Plus Olaparib (AZD2281) Administered Prior to Surgery in the Molecular Profile of Resectable Urothelial Bladder Cancer.
Estimated Study Start Date : October 2018
Estimated Primary Completion Date : December 2019
Estimated Study Completion Date : March 2020

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Bladder Cancer

Arm Intervention/treatment
Experimental: Durvalumab plus Olaparib
Durvalumab 1500 mg every 4 weeks for up to a maximum of 2 months (up to 2 doses/cycles) plus Olaparib 300 mg b.i.d. up to 56 days (2 cycles of 28 days each cycle).
Drug: Durvalumab
Infusion

Drug: Olaparib
P.O.




Primary Outcome Measures :
  1. Impact of neoadjuvant treatment with durvalumab plus olaparib in the molecular profile of resectable urothelial bladder cancer (Pathological complete response rate (pCRR)) [ Time Frame: 24 weeks ]
    pCRR will be analysed based on the percentage of patients who obtained a pathological complete response. Pathologic response will be evaluated on cystectomy tumor sample


Secondary Outcome Measures :
  1. Radiological response of durvalumab plus olaparib as presurgical treatment [ Time Frame: 16 weeks ]
    Radiological response will be assessed according to RECIST 1.1 criteria in patients with measurable and/or non-measurable disease at baseline that can be accurately assessed at baseline by computed tomography (CT) / magnetic resonance imaging (MRI) and is suitable for repeated assessment and previous to cystectomy. Patients without a radiologic post-baseline tumour assessment will be considered not evaluable for this endpoint.

  2. Toxicity profile of durvalumab plus olaparib as presurgical treatment in bladder cancer [ Time Frame: 28 weeks ]
    Percentage of patients with each of the adverse event per grade


Other Outcome Measures:
  1. Predictive and prognostic exploratory biomarkers in collected tumour tissue and plasma and their association with disease status and/or response/failure to study treatment [ Time Frame: 24 weeks ]
    Summary statistics and corresponding changes (or percent changes) from baseline tabulated by time and cohort



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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  1. Written informed consent obtained from the subject prior to performing any protocol related procedures, including screening evaluations
  2. Age ≥18 years at time of study entry
  3. Subjects with histological confirmation of T2-T4a urothelial bladder by transurethral resection
  4. Patients aimed for cystectomy without neoadjuvant chemotherapy
  5. Tumor tissue (archival or recent acquisition) from diagnostic Transurethral Resection (TUR) must be available (block or 5 - 15 unstained slides of formalin fixed paraffin embedded (FFPE) tissue) for correlative studies.
  6. Eastern Cooperative Oncology Group (ECOG) performance status of 0-1 Exclusion Criteria.
  7. Life expectancy of > 16 weeks
  8. Body weight > 30kg
  9. Normal organ and bone marrow function prior to administration of study treatment as defined below:

    • Haemoglobin > 10.0 g/dL with no blood transfusion in the past 28 days
    • Absolute neutrophil count (ANC) 1.5 x (> 1500 per mm3)
    • Platelet count ≥ 100 x 109/L (>100,000 per mm3)
    • Serum bilirubin ≤ 1.5 x institutional upper limit of normal (ULN).
    • Aspartate aminotransferase (AST)/ alanine aminotransferase (ALT) ≤ 2.5 x institutional upper limit of normal unless liver metastases are present, in which case it must be ≤ 5x ULN
    • Serum creatinine Clearance > 51 mL/min by the Cockcroft-Gault formula (Cockcroft and Gault 1976) or by 24-hour urine collection for determination of creatinine clearance.
  10. Evidence of post-menopausal status or negative urinary or serum pregnancy test for female pre-menopausal subjects within 28 days of study treatment and confirmed prior to treatment on day 1.
  11. Subject is willing and able to comply with the protocol for the duration of the study including undergoing treatment and scheduled visits and examinations.
  12. Male patients and their partners, who are sexually active and of childbearing potential, must agree to the use of two highly effective forms of contraception in combination, throughout the period of taking study treatment and for 180 days after last dose of study drug(s) to prevent pregnancy in a partner. Female patients of child bearing potential and male patients with partners of child bearing potential, who are sexually active, must agree to the use of two highly effective forms of contraception throughout period of taking study treatment and for 1 month (female patients) / 3 months (male patients) after last dose of study drug.
  13. At least one lesion (measurable and/or non-measurable) that can be accurately assessed at baseline by CT/MRI and is suitable for repeated assessment.
  14. Formalin fixed, paraffin embedded (FFPE) tumour sample from the primary cancer must be available for central testing. If there is not confirmation of the availability of an archived tumour sample prior to enrolment the patient is not eligible for the study

Exclusion criteria:

  1. Participation in another clinical study with an investigational product during the last 4 weeks
  2. Concurrent enrolment in another clinical study, unless it is an observational (non- interventional) clinical study or during the follow-up period of an interventional study
  3. Prior therapy with anti-PD-1, anti-PD-L1 including durvalumab, anti-PD-L2, anti-CD137, or anti-CTLA-4 antibody (or any other antibody or drug specifically targeting T-cell co- stimulation or checkpoint pathways).
  4. Receipt of the last dose of anti-cancer therapy (chemotherapy, immunotherapy, endocrine therapy, targeted therapy, biologic therapy, tumor embolization, monoclonal antibodies, other investigational agent) ≤ 28 days prior to the first dose of study drug.
  5. Resting electrocardiogram (ECG) with time between the start of the Q wave and the end of the T wave corrected for heart rate (QTc)> 470 msec on 2 or more time points within a 24 hour period or family history of long QT syndrome.
  6. Current or prior use of immunosuppressive medication within 28 days before the first dose of durvalumab, with the exceptions of intranasal and inhaled corticosteroids or systemic corticosteroids at physiological doses, which are not to exceed 10 mg/day of prednisone, or an equivalent corticosteroid.
  7. Any unresolved toxicity National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) Grade ≥1 from previous anticancer therapy with the exception of alopecia, vitiligo, and the laboratory values defined in the inclusion criteria
  8. Any concurrent chemotherapy, Investigational Product (IP), biologic, or hormonal therapy for cancer treatment. Concurrent use of hormonal therapy for non-cancer-related conditions (eg, hormone replacement therapy) is acceptable.
  9. Radiotherapy treatment to more than 30% of the bone marrow or with a wide field of radiation within 4 weeks of the first dose of study drug.
  10. Major surgical procedure (as defined by the Investigator) within 28 days prior to the first dose of IP and patients must have recovered from any effects of any major surgery.
  11. Previous allogenic bone marrow transplant or double umbilical cord blood transplant (dUCBT).
  12. Whole blood transfusions in the last 120 days prior to entry to the study (packed red blood cells and platelet transfusions are acceptable.
  13. Active or prior documented autoimmune or inflammatory disorders (including inflammatory bowel disease [eg, colitis or Crohn's disease], diverticulitis [with the exception of diverticulosis], systemic lupus erythematosus, Sarcoidosis syndrome, or Wegener syndrome [granulomatosis with polyangiitis, Graves' disease, rheumatoid arthritis, hypophysitis, uveitis, etc]).
  14. Patients considered a poor medical risk due to a serious, uncontrolled medical disorder, non- malignant systemic disease or active, uncontrolled infection.
  15. Past medical history of Interstitial Lung Disease (ILD), drug-induced ILD, radiation pneumonitis which required steroid treatment, or any evidence of clinically active ILD.
  16. Subjects with uncontrolled adrenal insufficiency
  17. Known drug or alcohol abuse
  18. History of another primary malignancy.
  19. Patients with symptomatic uncontrolled brain metastases.
  20. Active infection including tuberculosis (clinical evaluation that includes clinical history, physical examination and radiographic findings, and tuberculosis (TB) testing in line with local practice), hepatitis B (known positive Hepatitis B Virus (HBV) surface antigen (HBsAg) result), hepatitis C, or human immunodeficiency virus (positive HIV 1/2 antibodies). Subjects with a past or resolved HBV infection (defined as the presence of hepatitis B core (HBc) antibody [anti-HBc] and absence of HBsAg) are eligible. Subjects positive for hepatitis C, HIV, or immunocompromised patients are eligible only if polymerase chain reaction is negative for Hepatitis C Virus (HCV) RNA.
  21. Receipt of live attenuated vaccine within 30 days prior to the first dose of study treatment.
  22. Female subjects who are pregnant or breastfeeding or male or female subjects of reproductive potential who are not willing to employ effective birth control from screening to 180 days after the last dose of study treatment.
  23. Known allergy or hypersensitivity to any of the study drugs or any of the study drug excipients.
  24. Prior randomisation or treatment in a previous durvalumab and/or tremelimumab clinical study regardless of treatment arm assignment.
  25. Prisoners or subjects who are involuntarily incarcerated.
  26. Any previous treatment with poly ADP ribose polymerase (PARP) inhibitor, including olaparib.
  27. Concomitant use of known strong CYP3A inhibitors (eg. itraconazole, telithromycin, clarithromycin, protease inhibitors boosted with ritonavir or cobicistat, indinavir, saquinavir, nelfinavir, boceprevir, telaprevir) or moderate CYP3A inhibitors (eg. ciprofloxacin, erythromycin, diltiazem, fluconazole, verapamil). The required washout period prior to starting olaparib is 2 weeks.
  28. Concomitant use of known strong (eg. phenobarbital, enzalutamide, phenytoin, rifampicin, rifabutin, rifapentine, carbamazepine, nevirapine and St John's Wort) or moderate CYP3A inducers (eg. bosentan, efavirenz, modafinil). The required washout period prior to starting olaparib is 5 weeks for enzalutamide or phenobarbital and 3 weeks for other agents.
  29. Patients with myelodysplastic syndrome/acute myeloid leukaemia or with features suggestive of MyeloDysplatic Syndrome (MDS) / acute myeloid leukemia (AML).
  30. Patients unable to swallow orally administered medication and patients with gastrointestinal disorders likely to interfere with absorption of the study medication.
  31. Judgment by the investigator that the patient is unsuitable to participate in the study
  32. Involvement in the planning and/or conduct of the study (applies to both AstraZeneca staff and/or staff at the study site)
  33. Previous enrolment in the present study.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03534492


Contacts
Contact: Ana Moreno +34918166804 ana.moreno@apices.es
Contact: Isabel Grau

Locations
Spain
Hospital Universitario Central de Asturias Not yet recruiting
Oviedo, Asturias, Spain, 33006
Contact: Carlos Álvarez, MD         
Principal Investigator: Carlos Álvarez, MD         
ICO Badalona Not yet recruiting
Badalona, Barcelona, Spain, 08916
Contact: Albert Font, MD         
Principal Investigator: Albert Font, MD         
Clinica IMQ Zorrotzaurre Not yet recruiting
Bilbao, Spain
Contact: Ricardo Fernández-Rodríguez, MD         
Principal Investigator: Ricardo Fernández-Rodríguez, MD         
Hospital San Pedro de Alcántara Not yet recruiting
Cáceres, Spain
Contact: Ricardo Collado-Martín, MD         
Principal Investigator: Ricardo Collado-Martín, MD         
Hospital Universitario Lucus Augusti Not yet recruiting
Lugo, Spain, 27003
Contact: Sergio Vázquez, MD         
Principal Investigator: Sergio Vázquez, MD         
Hospital Ramón Y Cajal Not yet recruiting
Madrid, Spain, 28034
Contact: Pablo Gajate, MD         
Principal Investigator: Pablo Gajate, MD         
Hospital Universitario 12 de Octubre Not yet recruiting
Madrid, Spain, 28041
Contact: Guillermo de Velasco, MD         
Principal Investigator: Guillermo de Velasco, MD         
Hopsital Universitario Madrid Sanchinarro (CIOCC) Not yet recruiting
Madrid, Spain
Contact: Juan F Rodríguez, MD         
Principal Investigator: Juan F Rodríguez, MD         
Hospital Virgen Macarena Not yet recruiting
Sevilla, Spain
Contact: Juan A Virizuela, MD         
Principal Investigator: Juan A Virizuela, MD         
Hospital La Fe Not yet recruiting
Valencia, Spain
Contact: José Muñoz-Langa, MD         
Principal Investigator: José Muñoz-Langa, MD         
Sponsors and Collaborators
Spanish Oncology Genito-Urinary Group
AstraZeneca
Sistemas Genómicos
Apices Soluciones S.L.
Investigators
Principal Investigator: Jesús García-Donas, MD PhD Centro Integral Oncológico Clara Campal
Principal Investigator: Juan F Rodriguez-Moreno, MD Centro Integral Oncológico Clara Campal

Responsible Party: Spanish Oncology Genito-Urinary Group
ClinicalTrials.gov Identifier: NCT03534492     History of Changes
Other Study ID Numbers: SOGUG-2017-A-IEC(VEJ)-2
2017-002765-22 ( EudraCT Number )
First Posted: May 23, 2018    Key Record Dates
Last Update Posted: May 25, 2018
Last Verified: May 2018
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No

Keywords provided by Spanish Oncology Genito-Urinary Group:
urothelial
bladder cancer
olaparib
durvalumab

Additional relevant MeSH terms:
Urinary Bladder Neoplasms
Urologic Neoplasms
Urogenital Neoplasms
Neoplasms by Site
Neoplasms
Urinary Bladder Diseases
Urologic Diseases
Antibodies, Monoclonal
Olaparib
Immunologic Factors
Physiological Effects of Drugs
Poly(ADP-ribose) Polymerase Inhibitors
Enzyme Inhibitors
Molecular Mechanisms of Pharmacological Action
Antineoplastic Agents