A Phase 2 interventional study of Netupitant and Palonosetron in Chemotherapy-induced Nausea and Vomiting (CINV), sponsored by Helsinn Healthcare SA. Completed at 17 sites in 4 countries. Open to participants aged Up to 17 Years. Per ClinicalTrials.gov, last updated 2024-06-25.
Sponsored by Helsinn Healthcare SA · Phase 2, Interventional, and Prevention
This study is Phase 2 pharmacokinetic (PK) and pharmacodynamic (PD) dose-finding study of oral netupitant administered concomitantly with oral palonosetron in pediatric cancer patients for the prevention of nausea and vomiting associated with emetogenic chemotherapy. Two different netupitant dosages will be tested in patients aged from 3 months to \< 18 years: 1.33 mg/kg up to a maximum of 100 mg, and 4 mg/kg up to a maximum of 300 mg. All netupitant doses in all age classes will be concomitantly administered with palonosetron 20 μg/kg (up to a maximum dose of 1.5 mg) which is the IV palonosetron dose approved by USA FDA for the pediatric population. The primary objective is to investigate the PK/PD relationship between netupitant exposure (AUC, Cmax) and antiemetic efficacy (CR in delayed phase) after a single oral netupitant administration, concomitantly with oral palonosetron in pediatric cancer patients receiving Moderately Emetogenic Chemotherapy (MEC) or Highly Emetogenic Chemotherapy (HEC) cycles. Efficacy parameter to be used in the correlation is the proportion of patients with Complete Response (CR i.e., no emetic episodes and no rescue medication) during (> 24-120 h after the start of chemotherapy on Day 1).
The secondary objectives are to assess the safety and tolerability after single oral administration of netupitant given concomitantly with a single oral administration of palonosetron; to evaluate the pharmacokinetic (AUC, Cmax, tmax and t1/2) of oral palonosetron at the fixed dose of 20 μg/kg in pediatric patients with the concomitant administration of netupitant. A total of 92 pediatric cancer patients receiving either HEC or MEC will be enrolled in the study.
793 studies on the registry are indexed under Vomiting; 99 are open to participants now.
This study's enrollment of 67 is below the median of 103 across 673 interventional studies indexed under Vomiting.
Browse Vomiting studies →Helsinn Healthcare SA is the lead sponsor of 32 studies on the registry; 1 is open to participants now.
Of its 8 completed or terminated interventional studies of FDA-regulated products, 7 (88%) have results posted.
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Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.
Exclusion Criteria:
Patient who received any drug with potential anti-emetic effect within 24 h prior to the start of reference chemotherapy, including but not limited to:
NK1- receptor antagonists (e.g., aprepitant or any other new drug of this class); 5-HT3 receptor antagonists (e.g., ondansetron, granisetron, dolasetron, tropisetron, ramosetron); Benzamides (e.g., metoclopramide, alizapride); Phenothiazines (e.g., prochlorperazine, promethazine, perphenazine, fluphenazine, chlorpromazine, thiethylperazine); Benzodiazepines initiated 48 h prior to study drug administration or expected to be received within 120 h following initiation of chemotherapy, except for single doses of midazolam, temazepam or triazolam; Butyrophenones (e.g., droperidol, haloperidol); Anticholinergics (e.g., scopolamine, with the exception of inhaled anticholinergics for respiratory disorders e.g., ipratropium bromide); Antihistamines (e.g., diphenhydramine, cyclizine, hydroxyzine, chlorpheniramine, dimenhydrinate, meclizine); Domperidone; Mirtazapine; Olanzapine; Prescribed cannabinoids (e.g., tetrahydrocannabinol, nabilone); Over the Counter (OTC) antiemetics, OTC cold or OTC allergy medications; Herbal preparations containing ephedra or ginger.
Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
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Studies most often ask for 0–1 or 0–2. Your doctor gives the score; the WHO scale uses the same steps. The full scale also has 5, which records death.
Ways of preventing pregnancy. “Highly effective” methods fail less than 1% of the time a year when used correctly — for example an IUD or an implant.
Criteria usually say which methods count and how long to keep using them after the last dose, sometimes for male participants too. Some studies accept a partner’s vasectomy if it was confirmed successful and that person is the participant’s only sexual partner.
A reason a treatment, test or procedure should not be given to a particular person, such as an allergy, another illness or a medicine they take.
Anti-inflammatory medicines such as prednisone, prednisolone and dexamethasone — not the anabolic steroids used for muscle.
Studies differ in what they allow: check which steroid medicines, routes (tablets, injections, creams, inhalers, eye drops) and doses this study accepts.
A drug or device being studied in a clinical trial.
It may be new, or already approved and being studied for another use, dose or form. Criteria often leave out people who took part in another study of one within a recent period, commonly 30 days or five half-lives.
CYP3A is a group of enzymes, mainly CYP3A4, in the liver and gut that break down many medicines. Some medicines, supplements and foods (grapefruit, St John’s wort) slow them down or speed them up, which changes how much of a study drug stays in the body.
Studies list them so they can be avoided or switched; bring a list of everything you take, including supplements.
Judged by the study doctor to matter for your health or for the study. It is a doctor’s decision, so ask the study team if you are unsure whether something counts.
Informed consent
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
ECOG performance status
A scale of how much an illness limits everyday activity. For people being assessed to join a study, scores run from 0 (fully active) to 4; lower is more active.
Studies most often ask for 0–1 or 0–2. Your doctor gives the score; the WHO scale uses the same steps. The full scale also has 5, which records death.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Contraception
Ways of preventing pregnancy. “Highly effective” methods fail less than 1% of the time a year when used correctly — for example an IUD or an implant.
Criteria usually say which methods count and how long to keep using them after the last dose, sometimes for male participants too. Some studies accept a partner’s vasectomy if it was confirmed successful and that person is the participant’s only sexual partner.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Contraindication
A reason a treatment, test or procedure should not be given to a particular person, such as an allergy, another illness or a medicine they take.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Corticosteroids (steroids)
Anti-inflammatory medicines such as prednisone, prednisolone and dexamethasone — not the anabolic steroids used for muscle.
Studies differ in what they allow: check which steroid medicines, routes (tablets, injections, creams, inhalers, eye drops) and doses this study accepts.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Investigational drug or device
A drug or device being studied in a clinical trial.
It may be new, or already approved and being studied for another use, dose or form. Criteria often leave out people who took part in another study of one within a recent period, commonly 30 days or five half-lives.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
CYP3A (CYP3A4) inhibitors and inducers
CYP3A is a group of enzymes, mainly CYP3A4, in the liver and gut that break down many medicines. Some medicines, supplements and foods (grapefruit, St John’s wort) slow them down or speed them up, which changes how much of a study drug stays in the body.
Studies list them so they can be avoided or switched; bring a list of everything you take, including supplements.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Clinically significant
Judged by the study doctor to matter for your health or for the study. It is a doctor’s decision, so ask the study team if you are unsure whether something counts.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Single oral dose of Netupitant 1.33 mg/kg up to a maximum of 100 mg (for patients \< 3 months of age the netupitant dose will be 0.8 mg/kg) administered with single oral dose of 20 μg/kg palonosetron up to a maximum of 1.5 mg.
Drug: Netupitant · Drug: Palonosetron
Single oral dose of Netupitant 4 mg/kg up to a maximum of 300 mg (for patients \< 3 months of age the netupitant dose will be 2.4 mg/kg) administered with single oral dose 20 μg/kg palonosetron up to a maximum of 1.5 mg.
Drug: Netupitant · Drug: Palonosetron
Netupitant 1.33 mg/kg oral suspension up to a maximum of 100 mg
Palonosetron 20 μg/kg solution for oral use up to a maximum of 1.5 mg
Netupitant 4 mg/kg oral suspension up to a maximum of 300 mg
Palonosetron 20 μg/kg solution for oral use up to a maximum of 1.5 mg
Area Under the Plasma Concentration Versus Time Curve From Time Zero to Infinity (AUC0-inf) of Netupitant
Mean values of area under the plasma Concentration versus time curve from time zero to infinity (AUC0-inf) of netupitant after a single oral netupitant administration, concomitantly with oral palonosetron, in pediatric cancer patients receiving HEC or MEC cycles. AUC estimates are obtained by non-compartmental analysis of population model-predicted individual plasma concentration-time profiles.
Time frame: within 168 hours after netupitant administration. A sampling windows approach will be used by collecting a single blood sample from each patient in one of these time windows: from 2 to 8 h, from 24 to 48 h, from 72 to 96 h and from 120 to 168 h.
Maximum Plasma Concentration (Cmax) of Netupitant
Mean values of maximum plasma concentration (Cmax) of netupitant after a single oral netupitant administration, concomitantly with oral palonosetron, in pediatric cancer patients receiving HEC or MEC cycles. Cmax estimates are obtained by non-compartmental analysis of population model-predicted individual plasma concentration-time profiles
Time frame: within 168 hours after netupitant administration. A sampling windows approach will be used by collecting a single blood sample from each patient in one of these time windows: from 2 to 8 h, from 24 to 48 h, from 72 to 96 h and from 120 to 168 h
Exposure - Response Analysis for Netupitant
Exposure - Response analysis for netupitant performed by assessing the relationships between exposure parameters AUC0-inf and Cmax with the primary efficacy endpoint, i.e., the CR in the delayed phase. Graphical exposure-response analysis for netupitant performed by assessing the relationship between individual exposure parameters (AUC0-inf) and Cmax) with the primary efficacy endpoint, i.e the CR in the delayed phase.
Time frame: > 24-120 hours after the start of chemotherapy on Day 1
Percentage of Pediatric Patients With Complete Response During the Delayed Phase
Percentage of Pediatric Patients with complete response (CR, i.e., no emetic episodes and no rescue medication) during the delayed phase (\> 24 to 120 h after the start of chemotherapy on Day 1) after a single oral netupitant administration, concomitantly with oral palonosetron, in pediatric cancer patients receiving HEC or MEC cycles.
Time frame: > 24-120 hours after the start of chemotherapy on Day 1
| Milestone | Netupitant 1.33 mg/kg Plus Palonosetron | Netupitant 4 mg/kg Plus Palonosetron |
|---|---|---|
| Started | 34 | 33 |
| Completed | 34 | 32 |
| Not completed | 0 | 1 |
| Withdrew: Withdrawal by subject | 0 | 1 |
Mean values of area under the plasma Concentration versus time curve from time zero to infinity (AUC0-inf) of netupitant after a single oral netupitant administration, concomitantly with oral palonosetron, in pediatric cancer patients receiving HEC or MEC cycles. AUC estimates are obtained by non-compartmental analysis of population model-predicted individual plasma concentration-time profiles.
| ng*hr/mL | Netupitant 1.33 mg/kg Plus Palonosetron | Netupitant 4 mg/kg Plus Palonosetron |
|---|---|---|
| patients 1 month to <3 months of age | 4460 | — |
| patients 3 month to <6 months of age | 3849 ± 91.3 | 17340 ± 36.4 |
| patients 6 month to <1 year of age | 7637 ± 113 | 8617 ± 45.2 |
| patients 1 year to <2 years | 2276 ± 29.8 | 9886 ± 59.6 |
| patients 2 years to <5 years | 3135 ± 44.0 | 14404 ± 131 |
| patients 5 years to <12 years | 2676 ± 35.0 | 10154 ± 70.7 |
| patients 12 years to <18 years | 3107 ± 54.9 | 12266 ± 26.9 |
Mean values of maximum plasma concentration (Cmax) of netupitant after a single oral netupitant administration, concomitantly with oral palonosetron, in pediatric cancer patients receiving HEC or MEC cycles. Cmax estimates are obtained by non-compartmental analysis of population model-predicted individual plasma concentration-time profiles
| ng/mL | Netupitant 1.33 mg/kg Plus Palonosetron | Netupitant 4 mg/kg Plus Palonosetron |
|---|---|---|
| 1 month to <3 months | 60.8 ± NA | — |
| 3 months to <6 months | 76.0 ± 27.1 | 233 ± 4.25 |
| 6 months to <12 months | 133 ± 71.7 | 255 ± 31.2 |
| 1 year to <2 years | 69.5 ± 19.3 | 275 ± 38.2 |
| 2 years to <5 years | 74.0 ± 32.3 | 266 ± 55.0 |
| 5 years to <12 years | 67.9 ± 32.1 | 213 ± 20.1 |
| 12 years to <18 years | 76.8 ± 27.3 | 274 ± 15.6 |
Exposure - Response analysis for netupitant performed by assessing the relationships between exposure parameters AUC0-inf and Cmax with the primary efficacy endpoint, i.e., the CR in the delayed phase. Graphical exposure-response analysis for netupitant performed by assessing the relationship between individual exposure parameters (AUC0-inf) and Cmax) with the primary efficacy endpoint, i.e the CR in the delayed phase.
| Participants | Netupitant 1.33 mg/kg Plus Palonosetron or Netupitant 4 mg/kg Plus Palonosetron |
|---|---|
| number of participants with CR in delayed phase | 45 |
| number of participants with no CR in delayed phase | 19 |
Percentage of Pediatric Patients with complete response (CR, i.e., no emetic episodes and no rescue medication) during the delayed phase (\> 24 to 120 h after the start of chemotherapy on Day 1) after a single oral netupitant administration, concomitantly with oral palonosetron, in pediatric cancer patients receiving HEC or MEC cycles.
| Participants | Netupitant 1.33 mg/kg Plus Palonosetron | Netupitant 4 mg/kg Plus Palonosetron |
|---|---|---|
| Percentage of Pediatric Patients With Complete Response During the Delayed Phase | 24 | 22 |
Collected over From the first dose of study drug on Visit 2 (Day 1, inclusively) until Visit 5 (follow up, Day 14 [+3]). Non-serious events are listed at a 3% frequency threshold.
| Group | Deaths | Serious | Other |
|---|---|---|---|
| Netupitant 1.33 mg/kg Plus Palonosetron | 0/34 (0%) | 0/34 (0%) | 22/34 (64.7%) |
| Netupitant 4 mg/kg Plus Palonosetron | 0/32 (0%) | 3/32 (9.4%) | 22/32 (68.8%) |
| Event | Netupitant 1.33 mg/kg Plus Palonosetron | Netupitant 4 mg/kg Plus Palonosetron |
|---|---|---|
| Febrile neutropeniaBlood and lymphatic system disorders | 0/34 | 2/32 |
| StomatitisGastrointestinal disorders | 0/34 | 1/32 |
| Neutropenic sepsisInfections and infestations | 0/34 | 1/32 |
| Urinary tract infectionInfections and infestations | 0/34 | 1/32 |
| Event | Netupitant 1.33 mg/kg Plus Palonosetron | Netupitant 4 mg/kg Plus Palonosetron |
|---|---|---|
| ThrombocytopeniaBlood and lymphatic system disorders | 10/34 | 6/32 |
| AnaemiaBlood and lymphatic system disorders | 9/34 | 7/32 |
| LeukopeniaBlood and lymphatic system disorders | 8/34 | 4/32 |
| NeutropeniaBlood and lymphatic system disorders | 3/34 | 6/32 |
| StomatitisGastrointestinal disorders | 2/34 | 5/32 |
| PyrexiaGeneral disorders | 1/34 | 5/32 |
| Febrile neutropeniaBlood and lymphatic system disorders | 2/34 | 3/32 |
| VomitingGastrointestinal disorders | 2/34 | 3/32 |
| Alanine aminotransferase increasedInvestigations | 3/34 | 1/32 |
| NauseaGastrointestinal disorders | 1/34 | 2/32 |
Male and female pediatric cancer patients from birth up to \<18 years, who were scheduled to receive HEC or MEC to be administered as single-day chemotherapy on Day 1 only or for multiple days. All participants who received study drug. In netupitant 4 mg/kg arm 1 patient was withdrew from the study after randomization of study drug and was not treated with the study drug (the overall number of participants started in netupitant 4 mg/kg arm was 33 and 32 patients completed the study).
| Age, Continuous(years) | Netupitant 1.33 mg/kg Plus Palonosetron | Netupitant 4 mg/kg Plus Palonosetron | Total |
|---|---|---|---|
| Mean | 6.6 ± 6.29 | 5.6 ± 5.46 | 6.1 ± 5.88 |
| Age, Customized(Participants) | Netupitant 1.33 mg/kg Plus Palonosetron | Netupitant 4 mg/kg Plus Palonosetron | Total |
|---|---|---|---|
| 3 to <6 months | 3 | 2 | 5 |
| 6 to <12 months | 4 | 5 | 9 |
| 1 to <2 years | 3 | 4 | 7 |
| 2 to <5 years | 6 | 6 | 12 |
| 5 to <12 years | 8 | 8 | 16 |
| 12 to <18 years | 9 | 7 | 16 |
| 1 to <3 months | 1 | 0 | 1 |
| Sex: Female, Male(Participants) | Netupitant 1.33 mg/kg Plus Palonosetron | Netupitant 4 mg/kg Plus Palonosetron | Total |
|---|---|---|---|
| Female | 13 | 14 | 27 |
| Male | 21 | 18 | 39 |
| Race (NIH/OMB)(Participants) | Netupitant 1.33 mg/kg Plus Palonosetron | Netupitant 4 mg/kg Plus Palonosetron | Total |
|---|---|---|---|
| American Indian or Alaska Native | 0 | 0 | 0 |
| Asian | 0 | 1 | 1 |
| Native Hawaiian or Other Pacific Islander | 0 | 0 | 0 |
| Black or African American | 0 | 0 | 0 |
| White | 34 | 31 | 65 |
| More than one race | 0 | 0 | 0 |
| Unknown or Not Reported | 0 | 0 | 0 |
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Studies of the drugs tested here: Netupitant · Palonosetron