Ph I/II Trial of Systemic VSV-IFNβ-NIS in Combination With Checkpoint Inhibitor Therapy in Patients With Select Solid Tumors

Solid Tumor Clinical Trial

Official title:

Phase 1-2 Trial of Systemically Administered VSV-IFNβ-NIS in Combination With Checkpoint Inhibitor Therapy in Patients With Selected Solid Tumors

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT03647163
• Other study ID #: VYR-VSV2-202
• Status: Recruiting
• Phase: Phase 1/Phase 2
• Start date: April 9, 2019
• Est. completion date: December 1, 2024

Study information

• Verified date: July 2023
• Source: Vyriad, Inc.
• Contact: Jennifer Boughton
• Phone: 9085533135
• Email: JBoughton[@]vyriad.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The safety run-in portion of this study is designed to identify the optimal dose of VSV-IFNβ-NIS in combination with pembrolizumab in patients with solid tumors and follows the 3+3 design. The expansion portion will use one-sample binomial designs to assess the efficacy of the combination in patients with refractory NSCLC or NEC. The optimal dose (RP2D) determined in the dose escalation portion of the trial will be used for the expansion portion. The study has been conducted with a dose of 1.7 × 1010 as the recommended phase II dose in an expansion cohort of 10 patients with NSCLC. However, current data suggests that VSV-IFNβ-NIS doses of up to 1.7 × 1011 is safe and likely more efficacious. Thus, this study will test a second VSV-IFNβ-NIS dose level, 1.0x1011 TCID50. A safety assessment will be carried out after 3 patients are enrolled. If this dose schedule is well tolerated and virus PK are not negatively impacted, both the NSCLC and NEC expansion cohorts will open using this dose schedule. If 2 of the first 3 patients or 2 of the first 6 patients experience a DLT, the dose will be de-escalated to 5 x 1010. The safety run-in/dose escalation portion of this study is expected to require a minimum of 3 patients and a maximum of 18 patients (6 patients per dose level). The expansion portion of this study is expected to require a minimum of 10 per cohort. The NSCLC and NEC patients enrolled at the identified optimal dose in the dose escalation cohort would be included in the dose expansion cohort if they are evaluable for the primary endpoint in the expansion portion (4 dose escalation patients at the optimal dose are expected to roll over to the expansion). Therefore, the overall sample size will be a maximum of 40 patients.

Description:

All patients will be dosed with VSV-IFNβ-NIS on day 1. For Part A, Part B [Group 1], and Part C [Group 1] pembrolizumab will be administered on day 1 (concurrent pembrolizumab dosing). For Part A, and Parts B and C [Group 2] pembrolizumab may be administered on day 8 (delayed pembrolizumab dosing). pembrolizumab treatment will continue Q3W per the Keytruda® USPI, with efficacy evaluations after cycle 2 then every 9 weeks until PD.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 70
• Est. completion date: December 1, 2024
• Est. primary completion date: December 1, 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Histologically confirmed diagnosis of:
• Arm 1: dose level 1 and below: Advanced and/or metastatic solid tumors for which no existing options are felt to provide clinical benefit
• Arm 2: dose level 2: Advanced and/or metastatic NSCLC OR NEC in which radiological progression has been demonstrated during therapy with a PD-1/PD-L1 immune checkpoint inhibitor, and for which no existing options are felt to provide clinical benefit.
• Arm 3: Advanced and/or metastatic NEC in which radiological progression has been demonstrated during therapy with a PD-1/PD-L1 immune checkpoint inhibitor, and for which no existing options are felt to provide clinical benefit.
• Arm4: Advanced and/or metastatic NSCLC in which radiological progression has been demonstrated during therapy with a PD-1/PD-L1 immune checkpoint inhibitor, and for which no existing options are felt to provide clinical benefit.
• Measurable disease based on RECIST 1.1. The first 3 patients in the safety run-in phase do not need measurable disease. Part C: advanced NEC (neuroendocrine carcinoma based on histopathology according to WHO criteria. Patients with small cell carcinoma, large cell neuroendocrine carcinoma, and neuroendocrine carcinoma not otherwise specified, of any primary organ are eligible in which radiological progression has been demonstrated during therapy with a PD-(L)1 immune checkpoint inhibitor, and for which no existing options are felt to provide clinical benefit.
• Performance status of 0 or 1 on the ECOG Performance Scale.
• Life expectancy of >3 months if not on active anti-cancer therapy
• Willingness to provide biological samples required for the duration of the study including a fresh tumor biopsy sample (See Section 14.0).
• Adequate organ function using predefined laboratory values obtained =14 days prior to registration.
• Negative pregnancy test for female patients of childbearing potential
• Absence of active CNS involvement. NOTE: Pre-enrollment imaging of asymptomatic patients not mandatory
• Ability to provide written informed consent.

Exclusion Criteria:

• Availability of and patient acceptance of curative therapy.
• Recent or ongoing serious infection, including:

1. Any active Grade 3 or higher (per the NCI CTCAE, version 4.03) viral, bacterial, or fungal infection within 2 weeks of registration.

2. Known seropositivity for or active infection by the human immunodeficiency virus (HIV).

3. Acute hepatitis B or acute hepatitis C. Patients with chronic hepatitis B or hepatitis C may be enrolled provided their liver function is adequate as per section 3.17

4. Known history of active TB (Bacillus tuberculosis).

• Any serious health condition, which, in the opinion of the investigator, would place the patient at undue risk from the study, including uncontrolled hypertension and/or diabetes, clinically significant pulmonary disease (e.g., chronic obstructive pulmonary disease requiring hospitalization within 3 months) or neurological disorder (e.g., seizure disorder active within 3 months)
• Prior therapy within the following timeframe before the planned start of study

treatment as follows:

• Chemotherapy, small molecule inhibitors, radiation, interventional radiology procedure, and/or other investigational agent: =3 weeks or 5 half-lives, whichever is shorter
• Other monoclonal antibodies, antibody-drug conjugates, radioimmunoconjugates, or experimental therapies: =4 weeks (=3 weeks with documented disease progression)
• New York Heart Association classification III or IV, known symptomatic coronary artery disease, or symptoms of coronary artery disease on systems review, or known cardiac arrhythmias (atrial fibrillation or SVT) (Appendix II).
• Any known or suspected active organ-threatening autoimmune disease, such as inflammatory bowel disease, autoimmune hepatitis, lupus, or pneumonitis, with the exception of hypothyroidism and type 1 diabetes that are controlled with treatment.
• Immunodeficiency or immunosuppression, including systemic corticosteroids at >10mg/day prednisone or equivalent within 1 week prior to planned start of study treatment
• History of severe immune-mediated adverse reaction to immune checkpoint inhibitors.
• Toxicities from previous therapies that have not resolved to a grade 1 or less.
• History of non-infectious pneumonitis that required steroids, or current pneumonitis.
• High volume disease, as assessed clinically via parameters such as radiologic impression and tumor markers or LDH.
• Portal vein thrombosis involving more than intrahepatic portal vein branches:

thrombosis of the right or left portal vein branch or the bifurcation, partial or complete obstruction of the portal vein trunk.

• Known concurrent malignancy that is progressing or requires active treatment. EXCEPTIONS: basal cell carcinoma of the skin, squamous cell carcinoma of the skin, in-situ cervical cancer that has been treated with curative intent, prostate cancer confined to the prostate gland with Gleason score <6 or PSA <1, as well as any stage I cancer treated with curative intent or any prior cancer with a disease-free interval of =3 years.
• Other concurrent anti-cancer therapy (chemotherapy, immunotherapy, radiotherapy, or any ancillary therapy considered investigational (used for a non-FDA approved indication and in the context of a research investigation)).
• Has received a live vaccine within 30 days of planned start of study treatment. Seasonal influenza vaccines for injection are generally inactivated flu vaccines and are allowed; intranasal influenza vaccines (e.g., Flu-Mist) are live attenuated vaccines and are NOT allowed.
• Any of the following because this study involves an investigational agent whose genotoxic, mutagenic and teratogenic effects on the developing fetus and newborn are

unknown:

• Pregnant women or women of reproductive ability who are unwilling to use highly effective contraception
• Nursing women
• Men who are unwilling to use a condom (even if they have undergone a prior vasectomy) while having intercourse with any woman, while taking the drug and for 4 weeks after stopping treatment.

Related Conditions & MeSH terms

• Carcinoma, Neuroendocrine
• Neuroendocrine Carcinoma
• Non Small Cell Lung Cancer
• Solid Tumor

Intervention

Biological:
• VSV-IFNß-NIS
Intravenous oncolytic Vesicular stomatitis virus (VSV) expressing Interferon-beta (IFNß) and the sodium iodide symporter (NIS)
• Pembrolizumab
Pembrolizumab
• ipilimumab + nivolumab
Intravenous ipilimumab 1mg/kg in combination with nivolumab 360mg

Locations

Country	Name	City	State
United States	Cleveland Clinic Taussig Cancer Institute	Cleveland	Ohio
United States	Mayo Clinic	Rochester	Minnesota

Sponsors (2)

Lead Sponsor	Collaborator
Vyriad, Inc.	Mayo Clinic

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Expansion arms: Overall response rate (ORR)	proportion of patients in the analysis population who have complete response (CR) or partial response (PR) based on RECIST 1.1 imaging	43 days - 6 months
Primary	Safety run-in arm: Number of participants with treatment related adverse events (NCI CTCAE; Version 4.03)	Assessment of safety and toxicity of intravenous VSV-IFNß-NIS in combination with pembrolizumab therapy	21 days
Secondary	Overall Survival (OS)	Survival time is defined as the time from registration to death due to any cause.	6 months
Secondary	Progression Free Survival (PFS)	Progression-free survival is defined as the time from registration to the earliest date documentation of disease progression or death due to any cause	6 months
Secondary	Duration of response	defined for all evaluable patients who have achieved an objective response as the date at which the patient's earliest best objective status is first noted to be either a CR or PR to the earliest date progression is documented.	6 months
Secondary	Disease Control Rate (DCR)	proportion of patients in the analysis population who have complete response (CR), partial response (PR) or stable disease (SD) based on RECIST 1.1 imaging on day 43.	6 months
Secondary	Adverse events	All eligible patients that have initiated treatment will be considered evaluable for assessing adverse event rate(s). The maximum grade for each type of adverse event will be recorded for each patient.	6 months