Efficacy & Safety of rAd-IFN Administered With Celecoxib & Gemcitabine in Patients With Malignant Pleural Mesothelioma (INFINITE)

• ClinicalTrials.gov Identifier: NCT03710876
• Recruitment Status: Active, not recruiting
• First Posted: October 18, 2018
• Last Update Posted: October 26, 2021
• Sponsor: Trizell Ltd
• Collaborator: University of Pennsylvania
• Information provided by (Responsible Party): Trizell Ltd

Tracking Information

• First Submitted Date: June 22, 2018
• First Posted Date: October 18, 2018
• Last Update Posted Date: October 26, 2021
• Actual Study Start Date: January 21, 2019
• Estimated Primary Completion Date: November 2023 (Final data collection date for primary outcome measure)

Current Primary Outcome Measures (submitted: October 16, 2018)

Overall Survival [ Time Frame: 60 months ]

Time to death (from any cause) from randomization

• Original Primary Outcome Measures: Same as current

Current Secondary Outcome Measures (submitted: October 16, 2018)

• Survival rate [ Time Frame: 60 months ]
  Number of deaths (from any cause) from randomization
• Progression Free Survival [ Time Frame: 60 months ]
  Time from randomization to the time when the modified Response Evaluation Criteria in Solid Tumor criteria for disease progression are first met, or when death from any cause occurs
• Best response [ Time Frame: 60 months ]
  Best response after randomization (complete response, partial response, or stable disease)

• Original Secondary Outcome Measures: Same as current

Current Other Pre-specified Outcome Measures (submitted: October 16, 2018)

• Adverse Events Grade 3 or 4 [ Time Frame: 60 months ]
  To evaluate the number of patients with Common Terminology Criteria for Adverse Events Grade 3 or 4
• rAd-IFN-related viral DNA [ Time Frame: 60 months ]
  To evaluate post-treatment levels of rAd-IFN-related viral DNA in biological
• Quality of Life; EQ-5D-5L Health Questionnaire [ Time Frame: 60 months ]
  Change in total score and individual components of the EQ-5D-5L; Assessment of health status including:

  1. Mobility
  2. Self-Care
  3. Usual Activities
  4. Pain/ Discomfort
  5. Anxiety/ Depression
  6. Health Status (scale 0-100)
• Quality of Life; Lung Cancer Symptom Scale-Mesothelioma [ Time Frame: 60 months ]
  Change in total score and individual components of the Lung Cancer Symptom Scale-mesothelioma Assessment of symptoms including:

  1. Appetite
  2. Fatigue
  3. Coughing
  4. Shortness of Breath
  5. Pain
  6. Symptom Severity
  7. Normal Activities
  8. Quality of Life
• Adenovirus type 5 neutralizing antibodies [ Time Frame: 60 months ]
  Correlation between the presence of adenovirus type 5 neutralizing antibodies prior to treatment and survival (death from any cause)
• Serum Mesothelin and Fibulin-3 [ Time Frame: 60 months ]
  Correlation between pre- and post-treatment levels and treatment outcomes

• Original Other Pre-specified Outcome Measures: Same as current

Descriptive Information

• Brief Title: Efficacy & Safety of rAd-IFN Administered With Celecoxib & Gemcitabine in Patients With Malignant Pleural Mesothelioma
• Official Title: A Phase 3, Open-Label, Randomized, Parallel Group Study to Evaluate the Efficacy and Safety of Intrapleural Administration of Adenovirus-Delivered Interferon Alpha-2b (rAd-IFN) in Combination With Celecoxib and Gemcitabine in Patients With Malignant Pleural Mesothelioma

Brief Summary

This study will evaluate intrapleural administration of Adenovirus-Delivered Interferon Alpha-2b (rAd-IFN) in combination with Celecoxib and Gemcitabine in patients with histologically confirmed Malignant Pleural Mesothelioma (MPM) who have failed a minimum of 1 treatment regimen and a maximum of 2 treatment regimens, 1 of which must have been an anti-folate and platinum combination regimen.

Eligible patients will be randomized 1:1 to either:

1. Treatment group: rAd-IFN + Celecoxib followed by Gemcitabine
2. Control group: Celecoxib followed by Gemcitabine

Patients randomized to the treatment group will receive rAd-IFN administered into the pleural space via an Intrapleural catheter (IPC) or similar intrapleural device on study Day 1.

The primary objective of this study is to compare the overall survival (OS) associated with rAd IFN, when administered with celecoxib and gemcitabine, versus that associated with celecoxib and gemcitabine alone for the treatment of patients with MPM

Detailed Description

TITLE: A Phase 3, Open-Label, Randomized, Parallel Group Study to Evaluate the Efficacy and Safety of Intrapleural Administration of Adenovirus-Delivered Interferon Alpha-2b (rAd-IFN) in Combination with Celecoxib and Gemcitabine in Patients with Malignant Pleural Mesothelioma

PROTOCOL NUMBER: rAd-IFN-MM-301

STUDY DRUGS: Nadofaragene firadenovec (Recombinant adenovirus vector containing the human interferon alpha-2b gene: rAd-IFN), celecoxib, and gemcitabine

PHASE: 3

INDICATION: Malignant pleural mesothelioma (MPM)

SPONSOR: Trizell, Ltd.

SITES: Approximately 80 sites globally

OBJECTIVES:

The primary objective of this study is to compare the overall survival (OS) associated with rAd IFN, when administered with celecoxib and gemcitabine, versus that associated with celecoxib and gemcitabine alone for the treatment of patients with MPM who have failed a minimum of 1 treatment regimen and a maximum of 2 treatment regimens, 1 of which must have been an anti-folate and platinum combination regimen.

The secondary objectives of this study are:

• To compare between rAd-IFN, when administered with celecoxib and gemcitabine, versus that associated with celecoxib and gemcitabine alone for the treatment of patients with MPM who have failed a minimum of 1 treatment regimen and a maximum of 2 treatment regimens, 1 of which must have been an anti-folate and platinum combination regimen, with respect to:

  • Survival rate at 12 months and every 6 months thereafter;
  • Progression-free survival (PFS);
  • Best response (complete response, partial response, or stable disease); and
  • Safety of rAd-IFN; and
• To evaluate rAd-IFN, when administered with celecoxib and gemcitabine, in a sub-set of patients with MPM who have failed a minimum of 1 treatment regimen and a maximum of 2 treatment regimens, 1 of which must have been an anti-folate and platinum combination regimen, with respect to viral shedding and biodistribution.

The exploratory objectives of this study are:

• To compare between rAd-IFN, when administered with celecoxib and gemcitabine, versus that associated with celecoxib and gemcitabine alone for the treatment of patients with MPM who have failed a minimum of 1 treatment regimen and a maximum of 2 treatment regimens, 1 of which must have been an anti-folate and platinum combination regimen, with respect to:

• Health-related Quality-of-Life,
• The relationship between immunological status and response to treatment, and
• Biocorrelates of response to treatment.

POPULATION:

The population for this study is patients with histologically confirmed MPM of epithelioid or biphasic (predominantly [>50%] epithelioid) histology who have failed a minimum of 1 treatment regimen and a maximum of 2 treatment regimens, 1 of which must have been an anti-folate and platinum combination regimen.

STUDY DESIGN AND DURATION:

The study is an open-label, randomized, parallel group study conducted in patients with histologically confirmed MPM of epithelioid or biphasic (predominantly [>50%] epithelioid) histology who have failed a minimum of 1 treatment regimen and a maximum of 2 treatment regimens, 1 of which must have been an anti-folate and platinum combination regimen.

Screening assessments must be completed within 28 days of Study Day 1, and eligible patients will be randomized to either:

1. Treatment group: rAd-IFN (Study Day 1) + celecoxib (Study Days 1 to 14) + gemcitabine (Study Days 14 and 21 [i.e., Days 1 and 8 of the first gemcitabine treatment cycle], gemcitabine will be repeated every 3 weeks until disease progression/early termination [ET]); or
2. Control group: celecoxib (Study Days 1 to 14) + gemcitabine (Study Days 14 and 21 [i.e., Days 1 and 8 of the first gemcitabine treatment cycle], gemcitabine will be repeated every 3 weeks until disease progression/ET).

Treatment Phase Patients randomized to receive rAd-IFN (treatment group) will have an intrapleural catheter (IPC) or other intrapleural access device previously in place or inserted for the study, permitting drug administration to an accessible pleural space. The rAd-IFN will be diluted to a volume of 25 mL using sterile normal saline and will be administered directly to the pleural space via the IPC or similar device.

Patients will receive gemcitabine until disease progression/ET. All adverse events will be captured from the time of the main study's informed consent through 30 days after the last dose of study treatment (rAd-IFN, celecoxib, and/or gemcitabine). All treatment emergent adverse events (TEAEs) and serious adverse events (SAEs) will be followed until resolution or stabilization.

Survival Follow-Up Phase Following disease progression, patients will be followed every 3 months for survival. All previously recorded TEAEs and SAEs will be followed until resolution or stabilization.

DOSAGE FORMS AND ROUTE OF ADMINISTRATION:

Patients randomized to the treatment group will receive rAd-IFN (3 × E11 viral particles) on Day 1 of the study, diluted to a total volume of 25 mL using sterile normal saline and administered into the pleural space via an IPC or similar intrapleural device.

All study patients (treatment and control) will receive:

• Celecoxib administered at a dose of 400 mg twice daily orally on Days 1 to 14 of the study; and
• Gemcitabine starting on Study Day 14, using the following treatment regimen: 1250 mg/m2 administered intravenously on Days 1 and 8 of a 21-day gemcitabine cycle and continued every 3 weeks until disease progression/ET.

STATISTICAL ANALYSES:

The primary analysis of the primary endpoint is a comparison of the OS curves between the 2 groups using a log-rank test. The log-rank test will be stratified using the same variables used for stratifying the randomization.

Secondary analyses of the primary endpoint will include a comparison of the survival rates at various time points since randomization and a comparison of the median survival times. The effect of baseline covariates will be assessed by constructing a proportional hazard model. Exploratory analyses will include comparison of the survival curves by methods that do not rely on proportional hazards.

Secondary time-to-event endpoints will be analyzed in the same manner as the primary efficacy endpoint.

Categorical efficacy endpoints will be summarized and compared between groups using a Pearson's test, with the effect of baseline covariates assessed using logistic regression.

The nature, incidence, severity, relatedness, expectedness, seriousness, and outcome of TEAEs will be summarized by treatment group for safety analyses.

There are 2 interim analyses planned:

• Analysis for futility will be assessed upon reaching 123 deaths (estimated to occur 27 months after first patient first visit [FPFV]). Approximately half of the available Beta will be spent at this interim; and
• Analysis for efficacy will be assessed upon reaching 234 deaths (estimated to occur 45 months after FPFV). Approximately one-fifth of the available Alpha will be spent at this interim.

The final analysis will be assessed upon reaching 267 deaths (estimated to occur 60 months after FPFV).

SAMPLE SIZE DETERMINATION:

The planned sample size is approximately 300 patients. Based on a 1:1 randomization between treatment groups, a 2.5% one-sided significance level, and a predicted survival at 18 months of 35% in the rAd-IFN treatment group versus 20% in the control group, the study will have at least 90% power (after adjusting for the interim analyses) to detect a statistically significant difference between the treatment groups in the primary endpoint using the log-rank test.

The calculation was based on the assumptions that recruitment is uniform over 3 years and that all alive patients are followed-up for 2 years after the end of recruitment.

DATA AND SAFETY MONITORING BOARD:

An independent Data and Safety Monitoring Board (DSMB) will be convened for this study to monitor safety, efficacy, and study integrity. All aspects of the DSMB's scope of review and procedures will be detailed in a DSMB charter.

• Study Type: Interventional
• Study Phase: Phase 3
• Study Design: Allocation: Randomized; Intervention Model: Parallel Assignment; Masking: None (Open Label); Primary Purpose: Treatment
• Condition: Malignant Pleural Mesothelioma

Intervention

• Biological: rAd-IFN
  Adenovirus-Delivered Interferon Alpha-2b
  Other Name: Nadofaragene firadenovec
• Drug: Celecoxib Oral Product
  400 mg twice daily
  Other Name: COX II Inhibitor
• Drug: Gemcitabine
  1250 mg/m2 administered intravenously on Days 1 and 8 of a 21-day cycle and continued every 3 weeks until disease progression/ early termination
  Other Name: Chemotherapy

Study Arms

• Active Comparator: Treatment Group
  rAd-IFN (Study Day 1) + celecoxib oral product (Study Days 1 to 14) + gemcitabine (Study Days 14 and 21 [i.e., Days 1 and 8 of the first gemcitabine treatment cycle], gemcitabine will be repeated every 3 weeks until disease progression/early termination [ET]
  Interventions:

  • Biological: rAd-IFN
  • Drug: Celecoxib Oral Product
  • Drug: Gemcitabine
• Placebo Comparator: Control Group
  Celecoxib oral product (Study Days 1 to 14) + gemcitabine (Study Days 14 and 21 [i.e., Days 1 and 8 of the first gemcitabine treatment cycle], gemcitabine will be repeated every 3 weeks until disease progression/ET.
  Interventions:

  • Drug: Celecoxib Oral Product
  • Drug: Gemcitabine

• Publications *: Not Provided

Recruitment Information

• Recruitment Status: Active, not recruiting
• Actual Enrollment (submitted: October 25, 2021): 53
• Original Estimated Enrollment (submitted: October 16, 2018): 300
• Estimated Study Completion Date: November 2024
• Estimated Primary Completion Date: November 2023 (Final data collection date for primary outcome measure)

Eligibility Criteria

Inclusion Criteria

Patients who meet all of the following criteria will be eligible to participate in the study:

1. Aged 18 years or older at the time of consent;
2. Able to give informed consent;
3. Has a confirmed histological diagnosis of MPM with histological type epithelioid or biphasic (if biphasic, histology must be predominantly [50%] epithelioid). Histological diagnosis of MPM will be confirmed centrally using specimens or slides from tumor specimens obtained at the time of initial presentation or a subsequent procedure. Central confirmation of diagnosis with immunohistochemistry will be performed, and independent central confirmation will be required for study entry;
4. Measurable disease, per modified Response Evaluation Criteria in Solid Tumors [RECIST] 1.1 (see Section 7) for pleural mesothelioma;

5. Has received a minimum of 1 treatment regimen and a maximum of 2 treatment regimens, which may have been chemotherapeutic and/or immunotherapeutic treatment regimens for MPM which included at least 1 anti-folate and platinum combination regimen;

   • Adjuvant or neoadjuvant therapy represent 1 line of therapy each;
   • Patients who have undergone primary surgical resection and/or radiation therapy to the pulmonary site are eligible to participate. For clarity, surgical resection and/or radiation therapy to the pulmonary site are not exclusionary and are not considered a line of therapy;
   • Treatment that is split between pre-surgical resection and post-surgical resection and is the same regimen will be counted as 1 regimen. Patients meeting this condition should be discussed with the Medical Monitor prior to including the patient in the study;
6. Has a pleural space accessible for IPC or similar device insertion. Patients with a previously inserted IPC or similar device may be enrolled, and the pre-existing IPC or similar device can be used for vector administration as long as it is functional and has no evidence of local infection;
7. Life expectancy 12 weeks in the judgement of the Investigator;
8. Eastern Cooperative Oncology Group (ECOG) status of 1 or 0;

9. Female and male patients:

   • Female patients of childbearing potential must have a negative pregnancy test upon entry into this study and agree to use a highly effective method of contraception from Screening until 1 month after the last dose of gemcitabine;

     • Highly effective methods of contraception that result in a low failure rate (i.e., <1% per year) when used consistently and correctly include combined (estrogen and progestogen containing) hormonal contraception associated with inhibition of ovulation (oral, intravaginal, or transdermal), progestogen-only hormonal contraception associated with inhibition of ovulation (oral, injectable, or implantable), intrauterine device, intrauterine hormone-releasing system, bilateral tubal occlusion, vasectomized partner, or sexual abstinence;
     • True abstinence, when in line with the preferred and usual lifestyle of the patient, is considered a highly effective method only if defined as refraining from heterosexual intercourse during the entire period of study participation and for 1 month after the last dose of gemcitabine. The reliability of sexual abstinence needs to be evaluated in relation to the duration of the clinical study and the preferred and usual lifestyle of the patient. Periodic abstinence (e.g., calendar, ovulation, symptothermal, and post-ovulation method) and withdrawal are not acceptable methods of contraception; and
   • Female patients of non-childbearing potential must be either postmenopausal (no menstrual period for a minimum of 12 months) or surgically sterile upon entry into the study;
   • Male patients must be either surgically sterile or agree to use a double-barrier contraception method from Screening until 6 months after the last dose of gemcitabine; o Where available and in accordance with local practice, male patients must be advised to seek further advice regarding cryoconservation of sperm prior to gemcitabine treatment due to the possibility of infertility after therapy with gemcitabine; and

10. Adequate laboratory values at Screening:

    • Hemoglobin 9 g/dL;
    • White blood cell count 3500/µL;
    • Absolute neutrophil count 1500/µL;
    • • Platelet count 100,000/µL;
    • International normalized ratio (INR) and activated partial thromboplastin time (aPTT) below the upper limit of normal (ULN). It is expected that patients receiving anticoagulation therapy will not have INR and aPTT results that fall within normal limits. It is not intended to exclude these patients and, therefore, medical discretion is permitted for patients who have clinically acceptable results in regards to their current concomitant anticoagulant therapy;
    • Aspartate aminotransferase (AST) 3 × ULN;
    • Alanine aminotransferase (ALT) 3 × ULN;
    • Total bilirubin 2 × ULN;
    • Estimated glomerular filtration rate (calculated using the Modification of Diet in Renal Disease study equation [see Appendix B]) 50 mL/min/1.73 m2; and
    • Serum albumin 2.5 g/dL.

Exclusion Criteria

Patients who meet any of the following criteria will be excluded from participation in the study:

1. Is "treatment-naïve" (i.e., has not received at least 1 anti-folate and platinum combination regimen);
2. Has previously received 3 or more lines of systemic chemotherapeutic or immunotherapeutic treatment. Treatment that is split between pre-surgical resection and post-surgical resection and is the same regimen will be counted as 1 regimen. Patients meeting this condition should be discussed with the Medical Monitor prior to including the patient in the study;
3. Has previously received treatment with gemcitabine;
4. Has stage IV extrathoracic metastatic disease;
5. Inadequate pulmonary function of clinical significance as per Investigator review;
6. Clinically significant pericardial effusion (i.e., as judged by the Investigator and/or requiring drainage) detected by computed tomography (CT) scan at Screening. Standard of care CT scans completed within 2 weeks prior to Screening may be used in place of the Screening CT scan on a case by-case basis as agreed with the Medical Monitor;

7. Prior therapy(ies), if applicable, must be completed according to the criteria below prior to vector administration:

   • Cytotoxic chemotherapy, at least 21 days from last dose;
   • Non-cytotoxic chemotherapy (e.g., small molecule inhibitor), at least 14 days from last dose;
   • Monoclonal antibody, at least 30 days from last dose;
   • Non-antibody immunotherapy (e.g., tumor vaccine), at least 42 days from last dose;
   • Radiotherapy, at least 14 days from last local site radiotherapy;
   • Hematopoietic growth factor, at least 14 days from last dose; or
   • Study drug, 30 days or 5 half-lives, whichever is longer, from last dose;
8. Patient previously treated with IFNs (e.g., for chronic active hepatitis);
9. Suspected/known hypersensitivity to IFN-α2b or rAd-IFN (including any of its excipients);
10. Known hypersensitivity to celecoxib (including any of its excipients) or sulfonamides;
11. Known hypersensitivity to gemcitabine (including any of its excipients);

12. Impaired cardiac function or clinically significant cardiac disease including the following:

    • New York Heart Association class III or IV congestive heart failure;
    • Myocardial infarction within the last 12 months; and
    • Patients known to have impaired left ventricular ejection fraction per institutional standards and of clinical significance as per Investigator review;
13. Women who are pregnant or breastfeeding;
14. Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, depression, or psychiatric illness/social situations within the last 12 months;
15. Patients with active, known, or suspected auto-immune disease or a syndrome that requires systemic or immunosuppressive agents (oral prednisolone or equivalent at a dose of 10 mg per day is permitted); NOTE: patients with vitiligo, residual hypothyroidism due to auto immune disease only requiring hormone replacement, psoriasis not requiring systemic treatment, or conditions not expected to recur in the absence of an external trigger are permitted to enroll;
16. History of asthma, acute rhinitis, nasal polyps, angioneurotic edema, urticaria, or other allergic type reactions after taking acetylsalicylic acid or NSAIDs, including COX-2 inhibitors;
17. History of ulcer disease or gastrointestinal bleeding;
18. Uncontrolled or poorly controlled hypertension (i.e., blood pressure >160/100 mmHg) requiring 3 or more anti-hypertensive drugs;
19. Heart rate corrected QT interval using Fridericia's formula >470 ms on resting 12-lead electrocardiogram (ECG);
20. Patients receiving lithium;
21. Any significant disease which, in the opinion of the Investigator, would place the patient at increased risk of harm if he/she participated in the study;
22. History of a prior malignancy for which treatment was completed <2 years prior to Screening or for which the patient has continued evidence of disease, or concurrent malignancy that is clinically unstable and requires tumor-directed treatment;
23. Has a congenital or acquired immunodeficiency, including patients with known history of infection with human immunodeficiency virus;
24. Has both serum albumin 2.5 to 3.5 g/dL and total bilirubin >1.5 ULN;
25. History of clinically significant inflammatory bowel disease requiring systemic (parenteral) immunosuppressive therapy within 5 years prior to Screening; or
26. History of galactose intolerance, Lapp lactase deficiency, or glucose-galactose malabsorption.

Sex/Gender

• Sexes Eligible for Study: All

• Ages: 18 Years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Contacts: Contact information is only displayed when the study is recruiting subjects
• Listed Location Countries: Australia, Canada, France, Germany, Italy, Poland, Russian Federation, United Kingdom, United States

Administrative Information

• NCT Number: NCT03710876
• Other Study ID Numbers: rAd-IFN-MM-301; 2017-003169-82 ( EudraCT Number )
• Has Data Monitoring Committee: Yes

U.S. FDA-regulated Product

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

IPD Sharing Statement

• Plan to Share IPD: No

• Current Responsible Party: Trizell Ltd
• Original Responsible Party: Same as current
• Current Study Sponsor: Trizell Ltd
• Original Study Sponsor: Same as current
• Collaborators: University of Pennsylvania

Investigators

• Principal Investigator: Daniel Sterman, MD; NYU Langone Laura and Isaac Perlmutter Cancer Center

• PRS Account: Trizell Ltd
• Verification Date: October 2021