A Phase I/IIa, Multicenter, Open-Label Study of Nous-209 Genetic Vaccine for the Treatment of Microsatellite Unstable Solid Tumors.
Study Identifier:
NOUS-209-01
CT.gov Identifier:
EudraCT Identifier:
EU Trial (CTIS) Number:
Study Contact Information:
Recruitment Complete
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Study Summary
To evaluate prophylactic vaccine NOUS-209 in prevention of occurrence of cancer in Lynch Syndrome Carriers NOUS-209 as a therapeutic vaccine for cancers characterized by Microsatellite Instability (tumors containing abnormalities affecting DNA repair) To evaluate vaccine-induced immune responses, as well as preliminary signs of anti-tumor activity in enrolled patients. To evaluate safety, tolerability, pharmacokinetics, pharmacodynamics and immunogenicity, and to detect any preliminary evidence of anti-tumor activity of Nous-209 genetic polyvalent vaccine based on a heterologous prime/boost regimen composed of the GAd20-209-FSP used for priming and MVA-209-FSP used for boosting in patients with unresectable or metastatic Mismatch Repair Deficient (dMMR) or Microsatellite Instability High (MSI-H) colorectal cancer (CRC), gastric, gastro-esophageal junction (G-E junction) ) and endometrial tumors in sporadic or hereditary forms of the diseases. To determine the recommended phase 2 dose (RP2D) for IP in combination with the anti-PD-1 checkpoint inhibitor pembrolizumab in patients with unresectable or metastatic dMMR or MSI-H CRC, gastric, or G-E junction tumors. To detect any preliminary evidence of anti-tumor activity of Nous-209 genetic polyvalent vaccine based on a heterologous prime / boost regimen composed of the GAd20-209-FSP used for priming and MVA-209-FSP used for boosting in patients with unresectable or metastatic Mismatch Repair Deficient (dMMR) or Microsatellite Instability High (MSI-H) colorectal cancer (CRC), gastric, gastro-esophageal junction (G-E junction) and endometrial tumors in sporadic or hereditary forms of the diseases. To evaluate safety and tolerability of two dose levels (one log difference for both GAd and MVA) of Nous-209 genetic polyvalent vaccine in combination with the programmed death receptor-1 (PD-1)-blocking antibody pembrolizumab, to assess immunogenicity of the combination and to detect preliminary evidence of anti-tumor activity. To explore immune correlates potentially associated with the clinical outcome with the aim to address the Nous-209 contribution to the activity of pembrolizumab To evaluate safety and tolerability of two dose levels of the Nous-209 in combination with pembrolizumab, assesses immunogenicity and detects preliminary evidence of anti-tumor activity. To evaluate NOUS-209 in combination with anti-PD1 checkpoint inhibitor (CPI) pembrolizumab versus pembrolizumab alone. To assess the efficacy and safety of NOUS-209 in combination with pembrolizumab The Phase 2 study will include two cohorts in dMMR/MSI-H unresectable and metastatic colorectal cancer (CRC):A randomized cohort and a single arm cohort Response assessment is evaluated every 9 (+/-1) weeks by CT imaging, according to RECIST v1.1 criteria. ctDNA assessments are at baseline, 11, 28, 49, 79 weeks and at objective progression on study.
To report Phase II trial data of Nous-209 plus pembrolizumab for dMMR/MSI-H mCRC patients refractory to αPD-1 (best response of stable disease (SD) or better on prior αPD-1).
Medical Condition
The disease, disorder, syndrome, illness, or injury that is being studied. On ClinicalTrials.gov, conditions may also include other health-related issues, such as lifespan, quality of life, and health risks.
Phase
The stage of a clinical trial studying a drug or biological product, based on definitions developed by the U.S. Food and Drug Administration (FDA). The phase is based on the study's objective, the number of participants, and other characteristics. There are five phases: Early Phase 1 (formerly listed as Phase 0), Phase 1, Phase 2, Phase 3, and Phase 4. Not Applicable is used to describe trials without FDA-defined phases, including trials of devices or behavioral interventions.
I/II
Sex
Female & Male
Age
18 - 85 Years
Study Drug
Study Status
Indicates the current recruitment status or the expanded access status
Recruitment Complete
Requirements information
Inclusion criteria
- Inclusion Criteria for Cohort C (Phase II) In order to be eligible, the subject must: Have the ability to comprehend and willingness to provide written informed consent (ICF) for the study. Have previously proven microsatellite instability-high (MSI-H) or mismatch repair deficient (dMMR) status (confirmatory testing is not required); • dMMR/MSI Testing: Patients are eligible to the combined treatment based on previous diagnosis for dMMR/MSI status. dMMR/MSI status diagnosis should be performed locally by IHC or NGS or PCR based tests that are certified per local requirementss (Hara et al. 2018; Boland et al. 1998) CDx ™, 2017. Patients with locally advanced unresectable or metastatic, microsatellite instability high (MSI-H) or mismatch repair deficient (dMMR) CRC who are eligible for anti-PD-1 1st line of treatment. Patients may have received prior adjuvant chemotherapy for CRC as long as it was completed at least 6 months prior to Study Day
- Be ≥18 years of age on day of signing informed consent. Have a life expectancy of at least 6 months. Have a performance status of 0 - 1 on the Eastern Cooperative Oncology Group (ECOG) Performance Status. Have resolution of toxic effect(s) of the most recent prior chemotherapy to Grade 2 or less (except alopecia). If subject received major surgery or radiation therapy they must have recovered from the toxicity and/or complications from the intervention. Have adequate organ function as defined in the following tables (Table 1. Adequate Organ Function Laboratory Values ). Specimens must be collected within 10 days prior to the start of study treatment. If any hematological or chemistry values are outside the specified range during the initial screening, rescreening process may be conducted to reassess and ensure compliance with the adequate organ function criteria as outlined in Table 1. Not be previously treated with a (licensed or experimental) anti-PD-1 or anti-PD-L1 checkpoint inhibitor. If participating in translational reasearch [see Section 7.0.6 Translational research (only selected sites)], agree to have a biopsy at baseline from a lesion that can be biopsied with an acceptable clinical risk (as judged by the Investigator in discussion with the interventional radiologist or endoscopist). An older (not older than 6 months) FFPE specimen from locations not radiated prior to biopsy can be accepted. Furthermore, optionally agree to have another biopsy taken on-treatment if not representing an unacceptable clinical risk and/or if technically feasible as judged by the Investigator in discussion with the interventional radiologist or endoscopist. Have measurable disease per RECIST version 1.1. Patients with a prior or concurrent malignancy whose natural history or treatment does not have the potential to interfere with the safety or efficacy assessment of the investigational regimen are eligible for this trial. Females: not be pregnant (see Appendix 7: Contraceptive Guidance and Pregnancy Testing), not breastfeed, and must have at least one of the following conditions that apply: • Not a woman of childbearing potential (WOCBP) as defined in Appendix 7: Contraceptive Guidance and Pregnancy Testing OR • A WOCBP who agrees to use highly effective contraceptive methods as outlined in Appendix 7: Contraceptive Guidance and Pregnancy Testing during the treatment period and for at least 180 days after the last dose of study treatment and refrain from egg donation during this period. Fertile male patients: agree to use a contraceptive as detailed in Appendix 7: Contraceptive Guidance and Pregnancy Testing of this protocol during the treatment period and for at least 180 days after the last dose of study treatment and refrain from donating sperm during this period. Inclusion Criteria for Cohort D (Phase II): In order to be eligible, the subject must: Have the ability to comprehend and willingness to provide written informed consent (ICF) for the study. Have previously proven microsatellite instability-high (MSI-H) or mismatch repair deficient (dMMR) status (confirmatory testing is not required); dMMR/MSI Testing: Patients are eligible to the combined treatment based on previous diagnosis for dMMR/MSI status. dMMR/MSI status diagnosis should be performed locally, by IHC or NGS or PCR based tests that are certified per local requirements (Hara et al. 2018; Boland et al. 1998) CDx ™, 2017. Patients with locally advanced unresectable or metastatic MSI-H/dMMR CRC who have had radiographic progression (PD) after having a best response of stable disease (SD) or better on/after anti-PD-1 treatment. May have progressed on additional approved therapy. Be ≥18 years of age on day of signing informed consent. Have a life expectancy of at least 6 months. Have a performance status of 0 - 1 on the Eastern Cooperative Oncology Group (ECOG) Performance Status. Have resolution of toxic effect(s) of the most recent prior cancer therapies to Grade 2 or less (except alopecia). If patient received major surgery or radiation therapy they must have recovered from the toxicity and/or complications from the intervention. Have adequate hematological and blood chemistry values for Phase II as indicated in Table 1. Adequate Organ Function Laboratory Values. The specimens must be collected within 10 days prior to the start of study treatment. If any hematological or chemistry values are outside the specified range during the initial screening, rescreening process may be conducted to reassess and ensure adequate organ function criteria as outlined in Table 1. If participating in translational research [see Section 7.0.6 Translational research (only selected sites)], agree to have a biopsy at baseline from a lesion that can be biopsied with an acceptable clinical risk (as judged by the Investigator in discussion with the interventional radiologist or endoscopist). An older (not older than 6 months) FFPE specimen from locations not radiated prior to biopsy can be accepted. Furthermore, optionally agree to have another biopsy taken on-treatment if not representing an unacceptable clinical risk and/or if technically feasible as judged by the Investigator in discussion with the interventional radiologist or endoscopist. Have measurable disease per RECIST version 1.1. Patients with a prior or concurrent malignancy whose natural history or treatment does not have the potential to interfere with the safety or efficacy assessment of the investigational regimen are eligible for this trial. Females: not be pregnant (see Appendix 7: Contraceptive Guidance and Pregnancy Testing), not breastfeed, and must have at least one of the following conditions that apply: • Not a woman of childbearing potential (WOCBP) as defined in Appendix 7: Contraceptive Guidance and Pregnancy Testing OR • A WOCBP who agrees to use highly effective contraceptive methods as outlined in Appendix 7: Contraceptive Guidance and Pregnancy Testing during the treatment period and for at least 180 days after the last dose of study treatment and refrain from egg donation during this period. Male patients: agree to use a contraceptive as detailed in Appendix 7: Contraceptive Guidance and Pregnancy Testing of this protocol during the treatment period and for at least 180 days after the last dose of study treatment and refrain from donating sperm during this period. Table 1: Adequate Organ Function Laboratory Values Hematological Absolute neutrophil count (ANC) ≥1500/µL Platelets ≥100 000/µL Hemoglobin ≥9.0 g/dL or ≥5.6 mmol/L (1) Renal Creatinine OR Measured or calculated creatinine (2) clearance (GFR can also be used in place of creatinine or CrCl) ≤1.5 × ULN OR 30 mL/min for participant with creatinine levels >1.5 × institutional ULN Hepatic Total bilirubin ≤1.5 ×ULN OR direct bilirubin ≤ULN for participants with total bilirubin levels >1.5 × ULN AST (SGOT) and ALT (SGPT) ≤2.5 × ULN (≤5 × ULN for participants with liver metastases) Coagulation [Optional] International normalized ratio (INR) OR prothrombin time (PT) Activated partial thromboplastin time (aPTT) ≤1.5 × ULN unless participant is receiving anticoagulant therapy as long as PT or aPTT is within therapeutic range of intended use of anticoagulants ALT (SGPT)= alanine aminotransferase (serum glutamic pyruvic transaminase); AST (SGOT)= aspartate aminotransferase (serum glutamic oxaloacetic transaminase); GFR= glomerular filtration rate; ULN= upper limit of normal. Criteria must be met without packed red blood cell (pRBC) transfusion within the prior 2 weeks. Participants can be on stable dose of erythropoietin (≥ approximately 3 months). Creatinine clearance (CrCl) should be calculated per institutional standard. Note: This table includes eligibility-defining laboratory value requirements for treatment; laboratory value requirements should be adapted according to local regulations and guidelines for the administration of specific chemotherapies.
Exclusion criteria
- The patient must be excluded from participating in if he/she: Has a diagnosis of immunodeficiency, or is receiving chronic systemic steroid therapy (in dosing exceeding 10 mg daily of prednisone equivalent) or any other form of immunosuppressive therapy within 7 days prior to the first dose of study drug. Has known active central nervous system (CNS) metastases and/or carcinomatous meningitis. Patients with previously treated brain metastases may participate provided they are stable (have no evidence of progression by imaging for at least four weeks prior to the first dose of trial treatment and any worsening of neurologic symptoms with respect to baseline), have no evidence of new or enlarging brain metastases, and are not using steroids for at least 14 days prior to pembrolizumab. Is expected to require any form of systemic or localized antineoplastic therapy while on study other than the study drugs. Phase IIa and Cohort C only: Had prior adjuvant treatment with an anti-PD1, or PD-L1 or PD-L2 agent or an antibody targeting other immunoregulatory receptors or mechanisms. Cohort D only: discontinued prior therapy with a checkpoint inhibitor due to Grade 3, or higher, treatment-related toxicities. Had prior allogeinic tissue or solid organ transplant. Has a history of (non-infectious) pneumonitis / interstitial lung disease that required steroids or has current pneumonitis / interstitial lung disease. Has known history of HIV (HIV1/2 antibodies). HIV-infected participants must be on anti-retroviral therapy (ART) and have a well-controlled HIV infection/disease defined as: Participants on ART must have a CD4+ T-cell count >350 cells/mm3 at time of screening Participants on ART must have achieved and maintained virologic suppression defined as confirmed HIV RNA level below 50 copies/mL or the lower limit of qualification (below the limit of detection) using the locally available assay at the time of screening and for at least 12 weeks prior to screening. Participants on ART must have been on a stable regimen, without changes in drugs or dose modification, for at least 4 weeks prior to study entry (Day 1) HIV-infected participants with a history of Kaposi sarcoma and/or Multicentric Castleman Disease. Had prior radiotherapy within 2 weeks of enrollment, or within 4 weeks of enrollment in the case of radiation to central nervous system (CNS), which requires ≥4-week washout. Patients must have recovered from all radiation-related toxicities, not require corticosteroids, and not have had radiation pneumonitis. Note: A one-week washout is permitted for palliative radiation (≤2 weeks of radiotherapy) for non-CNS disease. Has immunosuppression implying the continued use of systemic (at prednisone dose equivalent of >10 mg) or topical steroids, at or near, the planned intramuscular injection site or the use of immunosuppressive agents for any concurrent condition in the 4 weeks prior to first study treatment administration. Inhaled and eye dropcontaining corticosteroids are permitted. Has received a live-virus vaccination within 30 days of pembrolizumab start. Seasonal flu vaccines that do not contain live virus are permitted. Covid-19 vaccines are permitted under the following guidance: mRNA Covid-19 vaccines are permitted if administered more than 2 weeks prior to Study Day 1, and Covid19 Adenovirusbased vaccines are accepted if administrated at least 6 months before Study Day 1. Administration of killed vaccines are allowed. Has an active severe infection requiring therapy. Has active HBV or HCV infection that requires treatment, or at risk for HBV reactivation (i.e., positive hepatitis B surface antigen [HBsAg]). Patients with negative HBsAg and positive total hepatitis B core antibody may be included if HBV DNA is undetectable at the time of screening. Patients who are positive for HCV antibody are eligible only if the PCR test is negative for HCV RNA. Patients with known current or prior HBV infection must have HBsAg and HBV DNA testing during screening and those with current or previous HCV infection must have HCV DNA testing. Has a chronic illness including, but not limited to, chronic heart failure, coronary heart disease, cardiac arrhythmias, or psychiatric illness/social situations that would limit compliance with study requirements. Has any history of anaphylaxis in reaction to a vaccination. Is a woman who is pregnant or breastfeeding. Any condition in the judgment of the Investigator, which makes the patient unsuitable for study participation; including psychological condition. Has known hypersensitivity to pembrolizumab or to components of the Nous-209 study therapy or its analogues (including a known history of allergy to egg proteins). History of another primary malignancy except for: Malignancy treated with curative intent and with no known active disease ≥5 years before the first dose of study treatment and of low potential risk for recurrence Adequately treated non-melanoma skin cancer or lentigo maligna without evidence of disease Adequately treated carcinoma in situ without evidence of disease. Participation in another clinical study with a study intervention or investigational medicinal device administered in the last 4 weeks prior to first dose of study treatment or concurrent enrolment in another clinical study. Has active tuberculosis infection (clinical evaluation that may include clinical history, physical examination and radiographic findings, or tuberculosis testing in line with local practice). Is receiving growth factors including, but not limited to, granulocyte colony stimulating factor (G-CSF), granulocyte macrophage-colony stimulating factor (GM-CSF), erythropoietin, etc., within 4 weeks of study drug administration. Revaccination Eligibility Criteria for participants receiving Nous-209 with pembrolizumab (Phase II) All participants that have been treated with Nous-209 and pembrolizumab combination in Phase IIa and in Phase IIb (Cohorts C and D) will be offered revaccination with Nous209 approximately 6 months after starting treatment (Table 3: Schedule of Activities for revaccination of eligible patients in Phase IIa and Phase IIb (Cohorts C and D)) providing the following criteria are met: Being in objective radiological stable disease according to RECIST v1.1 without any prior evidence of Partial response (PR), complete response (CR), or progressive disease (PD), based on the last available on-treatment scan prior to revaccination. Have no limiting toxicities preventing further administration of pembrolizumab (see Appendix 4: Management of Immune-Related Adverse Events). Continues to fufil the eligibility criteria for enrolment, except for the following inclusion criterion of Cohort C participants: 9. Not have been previously treated with a (licensed or experimental) anti-PD1 or anti-PD-L1 checkpoint inhibitor. Revaccination is not permitted for patients in Phase IIb Cohort C receiving pembrolizumab only. Participants who meet the criteria for revaccination may only receive revaccination once. During the revaccination period, participants will receive the same prime-boost vaccination doses and regimen of GAd20-209 FSP and MVA-209-FSP as in the original vaccination treatment period. Participants will continue to receive pembrolizumab at 200 mg Q3W. Image acquisitions and tumour assessments should continue on their regular imaging schedule for the duration of treatment (see Section 7.1 Schedule of Activities (SoA) (Phase II)).
Clinical Study Information for Healthcare Providers
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Study Locations
Location
Investigator
Status
Condition(s) Treated at Site
Location
START Madrid, Spain (CIOCC)
Madrid, Spain, 28050
Investigator
Juan José Soto
Status
Recruitment Complete
Condition(s) Treated at Site
Bowel (Colorectal)
Gastric
Solid Tumor
Esophageal