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A Multicenter Study Evaluating the Efficacy and Safety of Nivolumab and Ipilimumab in Combination With NP-101 Versus Placebo in Refractory Advanced and Metastatic Gastroenteropancreatic Neuroendocrine Carcinomas (GEP-NECs)

6 novembre 2026 mis à jour par: Novatek Pharmaceuticals

A Seamless Adaptive Randomized Phase 2/3, Double-Blind, Placebo-controlled, Multicenter Study Evaluating the Efficacy and Safety of Nivolumab and Ipilimumab in Combination With NP-101 Versus Placebo in Refractory Advanced and Metastatic Gastroenteropancreatic Neuroendocrine Carcinomas (GEP-NECs)

This clinical trial uses a study drug (NP-101) alone in some parts of the study or with a recommended treatment for GEP-NEC called Nivo/Ipi (a combination of Nivolumab and Ipilimumab) in other parts of the study and tests it against Placebo (look alike capsules with no active drug) with Nivo/Ipi. The study is divided into three parts. Participants will participate in only one of 3 study parts: Part 1- Dose escalation or Part 2 - Dose selection or Part 3 - Selected dose continuation.

The goal of this clinical trial is to learn if NP-101 (the study drug) can help people with poorly differentiated GEP-NEC live longer; the study includes males and females, age 18 and older who agree to join the study and who qualify.

The main questions the study seeks to answer:

  1. Is the study drug in combination with Nivo/Ipi safe?
  2. How does the body process the study drug alone and in combination with Nivo/Ipi?
  3. How does the body process the study drug with and without food?
  4. Can the study drug plus Nivo/Ipi (the recommended treatment) help people with GEP-NEC live longer than people who do not take the study drug, but who do receive recommended treatment?

Participants will be asked to report how they are feeling, allow for blood draws, body scans, visit the clinic for testing, allow for removal of tumor tissue, take study drug or capsules without medication (along with the recommended treatment) and other procedures which will be explained, along with the study visit schedule, in detail by the study staff before agreeing to participate.

Aperçu de l'étude

Type d'étude

Interventionnel

Inscription (Estimé)

381

Phase

  • Phase 2
  • Phase 3

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Coordonnées de l'étude

Sauvegarde des contacts de l'étude

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

18 ans et plus (Adulte, Adulte plus âgé)

Accepte les volontaires sains

Non

Sexes éligibles pour l'étude

Tout

La description

Inclusion Criteria:

  • Age >18 years.

  • Participants must have histologically or cytologically confirmed relapsed and/or refractory unresectable advanced and/or metastatic high-grade gastroenteropancreatic neuroendocrine carcinoma (GEP-NECs) and have failed at least one line of therapy.

  • Participants must have received at least one prior therapy for this disease, including platinum therapy. Participants must have recovered from acute toxicities of prior chemotherapy. Any prior non-hematologic vital organ toxicity (cardiac, pulmonary, hepatic, and renal) of previous therapy must have resolved to grade 1 or less. Neurological toxicities must have resolved to grade 2 or less.

  • Participants must have radiologic disease measurable by RECIST v1.1 criteria.

  • All previous chemotherapy, investigational drugs, or radiation must be completed at least three weeks prior to starting study treatment.

  • Performance status ECOG Performance status ≤ 2

  • Participants must have adequate organ and marrow function as defined by all the below parameters:

    • Hemoglobin ≥8.0g/dl
    • Absolute neutrophil count ≥1,000/µcL
    • Platelet count ≥70,000/µcL
    • Total bilirubin < 1.5 X institutional upper limit of normal (IULN).
    • AST (SGOT) ≤ 3 X IULN.
    • ALT (SGPT) ≤ 3 X IULN.
    • AST or ALT ≤ 5 × ULN for participants with liver metastases.
    • Calculated creatinine clearance ≥ 45 mL/min.
    • Serum albumin ≥ 25 g/L (2.5 g/dL)
  • Participants must have the ability to understand and the willingness to sign a written informed consent document.

  • Female participants of childbearing potential and male participants with a partner of childbearing potential must agree to practice reliable contraception or to practice abstinence for at least 28 days before starting treatment and for at least 60 days after the last dose of NP-101, and for at least 5 months after last dose of nivolumab and for at least 3 months after the last dose of ipilimumab, whichever is later. Reliable contraception is defined as:

One highly effective method and one additional effective (barrier) method:

Examples of highly effective methods:

  • Intrauterine device (IUD)
  • Hormonal (injections, implants, levonorgestrel releasing intrauterine system [IUS], medroxyprogesterone acetate depot injections, ovulation inhibitory progesterone-only pills [e.g., desogestrel])
  • Tubal ligation
  • Partner's vasectomy

Examples of additional effective methods:

  • Male condom

  • Diaphragm

  • Cervical Cap

  • Participants must agree to not donate eggs or sperm starting at screening and throughout the study period, and for at least 60 days after the last dose of NP-101, and for at least 5 months after the last dose of nivolumab and for at least 3 months after the last dose of ipilimumab, whichever is later The presence of any of the following will exclude a participant from study enrollment.

    • Pulmonary neuroendocrine carcinoma (Small cell or non-small cell) are excluded from this trial.
    • Well differentiated GEP-NETs are excluded from this trial.
    • Prior treatment toxicities that have not resolved to ≤ Grade 2 according to NCI CTCAE Version 5.0 (list exceptions, e.g. alopecia, neuropathy, etc.).
    • Participants received prior nivolumab or ipilimumab.
    • Participants with untreated brain metastases/CNS disease will be excluded from this clinical trial because of their poor prognosis and because they often develop progressive neurologic dysfunction that would confound the evaluation of neurologic and other adverse events. Participants with treated CNS metastases will be considered for the study.
    • History of allergic reactions attributed to compounds of similar chemical or biologic composition to NP-101 or immunotherapy (nivolumab or ipilimumab) used in this study.
    • Participants with uncontrolled intercurrent illness including, but not limited to ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements.
    • QT interval on an electrocardiogram (ECG) corrected for heart rate using Fridericia's formula (QTcF) > 470 ms (males) or > 480 ms (females) at screening (any 2 of 3 triplicate ECGs)
    • Solid organ or allogeneic hematopoietic stem cell transplant recipients.
    • Participants with significant autoimmune disease requiring immunosuppressive treatment, and participants with active interstitial lung disease or pneumonitis.
    • Participants who have a diagnosis of immunodeficiency or are receiving systemic steroid therapy or any other form of immunosuppressive therapy within 7 days prior to the first dose of study drug. The use of physiological doses of corticosteroids may be approved after consultation with the Sponsor. Examples of physiological doses of steroids include: Hydrocortisone: 10-25 mg total daily dose, Prednisone or Prednisolone: 4-10 mg daily, and Methylprednisolone: 3-5 mg daily.
    • Pregnant or breastfeeding women are excluded from this study.
    • Known chronic active untreated hepatitis B or C infection.
    • HIV-positive participants on combination antiretroviral therapy.
    • Participants with inflammatory bowel disease (such as Crohn's) that could affect the intestinal absorption of NP-101 capsules
    • Current use, or use within 14 days prior to first dose (or [5 half-lives / documented induction offset period], whichever is longer), of any strong or moderate inducer of CYP3A4, CYP1A2, CYP2C9, or CYP2D6, including but not limited to those listed in Table 7
    • Current use of any medication that is a sensitive substrate of CYP2C9, CYP3A4, CYP1A2, or CYP2D6 with a narrow therapeutic index (including but not limited to warfarin, phenytoin, and other agents listed in Table 8), unless an alternative non-interacting agent is available, or unless the Investigator/Medical Monitor determines the patient can be safely managed with enhanced monitoring (e.g., INR monitoring for warfarin, therapeutic drug level monitoring for phenytoin)

Exclusion Criteria:

  • The presence of any of the following will exclude a participant from study enrollment.

    • Pulmonary neuroendocrine carcinoma (Small cell or non-small cell) are excluded from this trial.
    • Well differentiated GEP-NETs are excluded from this trial.
    • Prior treatment toxicities that have not resolved to ≤ Grade 2 according to NCI CTCAE Version 5.0 (list exceptions, e.g. alopecia, neuropathy, etc.).
    • Participants received prior nivolumab or ipilimumab.
    • Participants with untreated brain metastases/CNS disease will be excluded from this clinical trial because of their poor prognosis and because they often develop progressive neurologic dysfunction that would confound the evaluation of neurologic and other adverse events. Participants with treated CNS metastases will be considered for the study.
    • History of allergic reactions attributed to compounds of similar chemical or biologic composition to NP-101 or immunotherapy (nivolumab or ipilimumab) used in this study.
    • Participants with uncontrolled intercurrent illness including, but not limited to ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements.
    • QT interval on an electrocardiogram (ECG) corrected for heart rate using Fridericia's formula (QTcF) > 470 ms (males) or > 480 ms (females) at screening (any 2 of 3 triplicate ECGs)
    • Solid organ or allogeneic hematopoietic stem cell transplant recipients.
    • Participants with significant autoimmune disease requiring immunosuppressive treatment, and participants with active interstitial lung disease or pneumonitis.
    • Participants who have a diagnosis of immunodeficiency or are receiving systemic steroid therapy or any other form of immunosuppressive therapy within 7 days prior to the first dose of study drug. The use of physiological doses of corticosteroids may be approved after consultation with the Sponsor. Examples of physiological doses of steroids include: Hydrocortisone: 10-25 mg total daily dose, Prednisone or Prednisolone: 4-10 mg daily, and Methylprednisolone: 3-5 mg daily.
    • Pregnant or breastfeeding women are excluded from this study.
    • Known chronic active untreated hepatitis B or C infection.
    • HIV-positive participants on combination antiretroviral therapy.
    • Participants with inflammatory bowel disease (such as Crohn's) that could affect the intestinal absorption of NP-101 capsules
    • Current use, or use within 14 days prior to first dose (or [5 half-lives / documented induction offset period], whichever is longer), of any strong or moderate inducer of CYP3A4, CYP1A2, CYP2C9, or CYP2D6, including but not limited to those listed in Table 7
    • Current use of any medication that is a sensitive substrate of CYP2C9, CYP3A4, CYP1A2, or CYP2D6 with a narrow therapeutic index (including but not limited to warfarin, phenytoin, and other agents listed in Table 8), unless an alternative non-interacting agent is available, or unless the Investigator/Medical Monitor determines the patient can be safely managed with enhanced monitoring (e.g., INR monitoring for warfarin, therapeutic drug level monitoring for phenytoin)

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Traitement
  • Répartition: Randomisé
  • Modèle interventionnel: Affectation parallèle
  • Masquage: Quadruple

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Comparateur placebo: Placebo

A GMP manufactured enteric capsule containing corn oil. Closely matched to NP-101 in size, shape, color and viscosity of API.

Non-experimental treatment intervention for GEP-NEC

Expérimental: Low Dose NP-101

The low dose will be determined during Part I of the study so the actual dosage cannot be specified at the time of posting.

Non-experimental treatment intervention for GEP-NEC

NP-101 is a GMP manufactured enteric capsule containing 600 mg of active pharmaceutical ingredient derived from a botanical source.

Expérimental: High Dose NP-101

The high dose will be determined during Part I of the study so the actual dosage cannot be specified at the time of posting.

Non-experimental treatment intervention for GEP-NEC

NP-101 is a GMP manufactured enteric capsule containing 600 mg of active pharmaceutical ingredient derived from a botanical source.

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Part I Primary Safety Objective
Délai: The DLT evaluation period for each participant is the first 28 days

To evaluate the safety of escalating doses of NP-101 combined with Nivo/Ipi. Corresponding Safety Endpoint: Determine incidence of dose-limiting toxicities (DLTs) of NP-101 combined with nivolumab and ipilimumab (Nivo/Ipi) to determine the recommended dose range of NP-101 (dose range of 2 doses will be selected) for study Part 2. Incidence and severity and attribution of adverse events (AEs) and serious adverse events (SAEs), clinical and laboratory, with severity assessed per the National Cancer Institute Common Terminology Criteria for Adverse Events, Version 5.0 (NCI CTCAE v5.0).

The DLT evaluation period for each participant is the first 28 days
Part I Pharmacokinetic Objective
Délai: PK sampling will occur at various timepoints and frequencies for the first 16 weeks.

To characterize the pharmacokinetic (PK) profile of NP-101 when given alone, and in combination with Nivo/Ipi. Corresponding Pharmacokinetic Endpoint: Serum concentration of thymoquinone at specified timepoints.

PK sampling will occur at various timepoints and frequencies for the first 16 weeks.
Part 2 - Primary Efficacy Objective
Délai: Response will be defined by participant response at 8 weeks.

To evaluate and compare the efficacy of 2 doses of NP-101 combined with Nivo/Ipi and select the dose to move forward to Part 3. Corresponding Efficacy Endpoint: Response will be defined by the Objective Response Rate (ORR) at 8 weeks, defined as the percentage of complete responses (CR) or partial responses (PR), as determined by the investigator review according to Response Evaluation Criteria in Solid Tumors (RECIST) v1.1. Response to treatment in the low and high dose group will be used for dose selection to move forward to Part 3.

Response will be defined by participant response at 8 weeks.
Part 2/Part 3 Primary Efficacy Objective
Délai: The maximum participation could be up to the final safety follow-up visit which occurs 90 days after last dose. Assuming survival the maximum time could be up to Study Day 821.

Primary Efficacy Objective of Part 2/Part 3: To evaluate the efficacy of the selected dose of NP-101 combined with Nivo/Ipi compared with Placebo combined with Nivo/Ipi. Corresponding Efficacy Endpoint: Overall survival (OS), defined as the time from randomization to death from any cause. Participants who are alive at the time of analysis, or who are lost to follow-up or withdrawn, will be censored at the date they were last known to be alive. Analysis Timepoints: When 130, 195 and 260 Events are observed in the primary analysis populations. Primary analysis participants are those randomized to control or the selected dose across Part 2 (80 participants; 40 of the selected dose and 40 control) and Part 3. A test for superiority of NP-101 arm over the placebo arm will be conducted.

The maximum participation could be up to the final safety follow-up visit which occurs 90 days after last dose. Assuming survival the maximum time could be up to Study Day 821.
Part 2/3 Pharmacokinetic Objective
Délai: Participants in Part 2/3 would participate in the PK sampling until the last day of cycle 4 (Each cycle is 28 days) which for Part2/3 would be Study Day 112

To evaluate the efficacy of the selected dose of NP-101 combined with Nivo/Ipi compared with Placebo combined with Nivo/Ipi. Corresponding Secondary Efficacy Endpoint: Serum concentration of thymoquinone at specified timepoints.

Participants in Part 2/3 would participate in the PK sampling until the last day of cycle 4 (Each cycle is 28 days) which for Part2/3 would be Study Day 112

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Part 2/Part 3 Secondary Efficacy Objective
Délai: Week 24

To evaluate the efficacy of the selected dose of NP-101 combined with Nivo/Ipi compared with Placebo combined with Nivo/Ipi.

Corresponding Secondary Efficacy endpoint:

Objective Response Rate (ORR) defined as the percentage of partial responses [PR] and complete responses [CR], as determined by the investigator review according to Response Evaluation Criteria in Solid Tumors (RECIST) v1.1. The difference in the ORR between the two arms will be calculated. Objective Response Rate (ORR) defined as the percentage of partial responses [PR] and complete responses [CR], as determined by the BICR according to Response Evaluation Criteria in Solid Tumors (RECIST) v1.1. The difference in the ORR between the two arms will be calculated. Confirmed ORR at week 24, defined as the proportion of participants with BICR confirmed CR or PR as best overall response through Week 24, prior to disease progression, death, or initiation of a new therapy. Progression-free survival (PFS), defined

Week 24
Secondary Objective Part 2/3 Patient Reported Outcomes
Délai: From randomization to first deterioration in the patient reported HRQoL/GHS and function (physical, role) scales of the EORTC QLQ-C30, maintained for two consecutive assessments or one assessment followed by death from any cause within 3 weeks.

To evaluate patient-reported outcomes (PROs) of disease or treatment-related symptoms, health-related quality of life (HRQoL) and global health status (GHS), and body function, experienced by participants on all treatment arms, as measured by the European Organization for Research and Treatment of Cancer quality-of-life questionnaire for cancer (EORTC QLQ-C30). To estimate time to deterioration, defined as the time from randomization to first deterioration (decrease from baseline of ≥10 points) in the patient reported HRQoL/GHS and function (physical, role) scales of the EORTC QLQ-C30, maintained for two consecutive assessments or one assessment followed by death from any cause within 3 weeks.

The EORTC QLQ-C30 scales and single-item measures convert to scores ranging from 0 (minimum) to 100 (maximum). However, the interpretation of higher scores varies: Global Health Status / Quality of Life: Higher scores indicate better overall quality of life.

From randomization to first deterioration in the patient reported HRQoL/GHS and function (physical, role) scales of the EORTC QLQ-C30, maintained for two consecutive assessments or one assessment followed by death from any cause within 3 weeks.

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Les enquêteurs

  • Chaise d'étude: Ahmed O Kaseb, MD, Co-Founder, Novatek Pharmaceuticals, Inc

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Estimé)

1 janvier 2027

Achèvement primaire (Estimé)

1 décembre 2029

Achèvement de l'étude (Estimé)

1 juin 2031

Dates d'inscription aux études

Première soumission

6 octobre 2026

Première soumission répondant aux critères de contrôle qualité

6 novembre 2026

Première publication (Réel)

13 novembre 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

13 novembre 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

6 novembre 2026

Dernière vérification

1 novembre 2026

Plus d'information

Termes liés à cette étude

Plan pour les données individuelles des participants (IPD)

Prévoyez-vous de partager les données individuelles des participants (DPI) ?

NON

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Oui

Étudie un produit d'appareil réglementé par la FDA américaine

Non

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