ClinicalTrials.gg
CompletedNCT03204279CINVUpdated Jun 25, 2024Results posted

PK/PD Study of Netupitant and Palonosetron in Pediatric Patients for Prevention of Chemotherapy-induced Nausea and Vomiting

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

Phase
Phase 2
Study type
Interventional
Enrollment
67
Allocation
Randomized
Ages
Up to 17 Years
Sex
All
01

Study summary

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.

02

Conditions studied

  • Chemotherapy-induced Nausea and Vomiting (CINV)

Browse trials for

03

In context

Vomiting

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 →

Lead sponsor

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.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Up to 17 Years
Sexes eligible
All
Accepts healthy volunteers
No

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.

Inclusion criteria

  1. Signed written by parent(s)/legal guardians of the pediatric patient in compliance with the local laws and regulations. In addition signed children's assent form according to local requirements.
  2. Male or female in- or out-patient from birth to \< 18 years at the time of randomization.
  3. Patient weight at least 3.3 kg.
  4. Naïve or non-naïve patient with histologically, and/or cytologically (or imaging in the case of brain tumors) confirmed malignant disease.
  5. Scheduled and eligible to receive at least one moderately or highly emetogenic chemotherapeutic agent on Day 1 only or for multiple days.
  6. For patient aged ≥ 10 years: Performance Status (ECOG PS) ≤ 2.
  7. For patient aged 2 years with known mild to moderate hepatic impairment: in the Investigator's opinion the impairment does not jeopardize patient's safety during the study.
  8. For patient aged 2 years with known mild to moderate renal impairment: in the Investigator's opinion the impairment should not jeopardize patient's safety during the study.
  9. For patient with known history or predisposition to cardiac abnormalities: in the Investigator's opinion the history/predisposition should not jeopardize patient's safety during the study.
  10. If the patient is female, she shall: a) not have attained menarche yet or b) have attained menarche and have a negative pregnancy test at the screening visit and at Day 1.
  11. Male or female fertile patient using reliable measures (such measures, for patient and sexual partner, include: implants, injectables, combined oral contraceptives, intrauterine devices, vasectomized/sterilized partner, use of a double-barrier method or sexual abstinence). The patient and his/her parent(s)/legal guardians must be counseled on the importance of avoiding pregnancy before or during the study.

Exclusion criteria

Exclusion Criteria:

  1. The patient and/or parents/caregivers are expected by the Investigator to be non-compliant with the study procedures.
  2. Patient has received or is scheduled to receive total body irradiation, total nodal irradiation, upper abdomen radiotherapy, half or upper body irradiation, radiotherapy of the cranium, craniospinal regions, head and neck, lower thorax region or the pelvis within 1 week prior to study entry (Day 1) or within 120 h after start of chemotherapy administration on Day 1.
  3. Known history of allergy to any component or other to any Neurokinin-1 (NK1) or 5-hydroxytryptamine 3 (5-HT3) receptor antagonists.
  4. Active infection.
  5. Uncontrolled medical condition (e.g., uncontrolled insulin dependent diabetes mellitus).
  6. Patient suffering from ongoing vomiting from any organic etiology (including patients with history of gastric outlet obstruction or intestinal obstruction due to adhesions or volvulus, patients with a symptomatic central nervous system(CNS) tumor causing nausea and/or vomiting) or patient with hydrocephalus.
  7. Patient who experienced any vomiting, retching, or nausea within 24 h prior to the administration of the study drug
  8. 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.

  9. Patient who received palonosetron within 1 week prior to administration of study drug.
  10. Patient who has been started on systemic therapy within 72 h prior to study drug administration or is planned to receive a corticosteroid as part of the chemotherapy regimen
  11. Patient aged \< 6 years who received any drug (defined as a medication with no marketing authorization granted for any age class and any indication) within 90 days prior to Day 1, or patient aged 6 years who received any investigational drug within 30 days prior to Day 1 or is expected to receive investigational drugs prior to study completion.
  12. Intake of alcohol, food or beverages (e.g., grapefruit, cranberry, pomegranate and aloe vera juices, German chamomile) known to interfere with either or CYP2D6 metabolic enzymes within 1 week prior to Day 1 and during the overall study period.
  13. Use of any drugs or substances known to be strong or moderate inhibitors of CYP3A4 and CYP2D6 enzymes within 1 week prior to Day 1 or planned to be used during the overall study period.
  14. Use of any drugs or substances known to be CYP3A4 substrates with narrow therapeutic range within 1 week prior to Day 1, or planned to be used during the overall study period.
  15. Use of any drugs or substances known to be inducers of CYP3A4 enzymes within 4 weeks prior to Day 1 or planned to be used during the overall study period.
  16. Lactating female patient.
  17. Patient with abnormal laboratory values that in the Investigator's opinion jeopardize the patient's safety during the study.
  18. Patient aged \< 2 years with known hepatic impairment (any grade), or patient aged 2 years with known severe hepatic impairment.
  19. Patient aged \< 2 years with known renal impairment (any grade), or patient aged 2 years with known severe renal impairment.
  20. Enrolment in a previous study with netupitant (either alone or in combination with palonosetron).
Terms in these criteria, in plain language(8)

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.

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.

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.

0
Fully active, no restrictions.
1
Limited in strenuous activity, but walking and able to do light work, such as housework or office work.
2
Walking and able to look after yourself, but unable to work; up and about more than half of waking hours.
3
Able to look after yourself only in part; in bed or a chair more than half of waking hours.
4
Unable to look after yourself at all; in bed or a chair all day.

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.

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.

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.

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.

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.

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.

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.

05

Study design

Phase
Phase 2
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Triple (Participant, Care provider, Investigator)
Enrollment
67 participants (actual)

Study arms

  • Experimental
    Netupitant 1.33 mg/kg plus Palonosetron

    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

  • Experimental
    Netupitant 4 mg/kg plus 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

Interventions

  • 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

06

What researchers measure

Primary outcomes

  1. 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.

  2. 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

  3. 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

Secondary outcomes

  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

07

Results

Posted Dec 7, 2020

Participant flow

Participant flow — Overall Study
MilestoneNetupitant 1.33 mg/kg Plus PalonosetronNetupitant 4 mg/kg Plus Palonosetron
Started3433
Completed3432
Not completed01
Withdrew: Withdrawal by subject01

Outcome measures

PrimaryArea 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.
Reported as:
Mean · ng*hr/mL
Area Under the Plasma Concentration Versus Time Curve From Time Zero to Infinity (AUC0-inf) of Netupitant
ng*hr/mLNetupitant 1.33 mg/kg Plus PalonosetronNetupitant 4 mg/kg Plus Palonosetron
patients 1 month to <3 months of age4460—
patients 3 month to <6 months of age3849 ± 91.317340 ± 36.4
patients 6 month to <1 year of age7637 ± 1138617 ± 45.2
patients 1 year to <2 years2276 ± 29.89886 ± 59.6
patients 2 years to <5 years3135 ± 44.014404 ± 131
patients 5 years to <12 years2676 ± 35.010154 ± 70.7
patients 12 years to <18 years3107 ± 54.912266 ± 26.9
PrimaryMaximum 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
Reported as:
Mean · ng/mL
Maximum Plasma Concentration (Cmax) of Netupitant
ng/mLNetupitant 1.33 mg/kg Plus PalonosetronNetupitant 4 mg/kg Plus Palonosetron
1 month to <3 months60.8 ± NA—
3 months to <6 months76.0 ± 27.1233 ± 4.25
6 months to <12 months133 ± 71.7255 ± 31.2
1 year to <2 years69.5 ± 19.3275 ± 38.2
2 years to <5 years74.0 ± 32.3266 ± 55.0
5 years to <12 years67.9 ± 32.1213 ± 20.1
12 years to <18 years76.8 ± 27.3274 ± 15.6
PrimaryExposure - 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
Reported as:
Count of participants · Participants
Exposure - Response Analysis for Netupitant
ParticipantsNetupitant 1.33 mg/kg Plus Palonosetron or Netupitant 4 mg/kg Plus Palonosetron
number of participants with CR in delayed phase45
number of participants with no CR in delayed phase19
Statistical analysis
  • Netupitant 1.33 mg/kg Plus Palonosetron or Netupitant 4 mg/kg Plus Palonosetron · loess (Local regression or polynomial) · p = 0.55 (CR in the delayed phase vs AUC0-inf) · Pearson r: 0.076R is the Pearson correlation is a coefficient statistic that measures linear correlation between two variables CR in the delayed phase vs AUC0-inf
  • Netupitant 1.33 mg/kg Plus Palonosetron or Netupitant 4 mg/kg Plus Palonosetron · loess (Local regression or polynomial) · p = 0.75 (CR in the delayed phase vs Cmax) · Pearson r: -0.041R is the Pearson correlation is a coefficient statistic that measures linear correlation between two variables CR in the delayed phase vs Cmax
SecondaryPercentage 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
Reported as:
Count of participants · Participants
Percentage of Pediatric Patients With Complete Response During the Delayed Phase
ParticipantsNetupitant 1.33 mg/kg Plus PalonosetronNetupitant 4 mg/kg Plus Palonosetron
Percentage of Pediatric Patients With Complete Response During the Delayed Phase2422

Adverse events

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.

Adverse event summary by group
GroupDeathsSeriousOther
Netupitant 1.33 mg/kg Plus Palonosetron0/34 (0%)0/34 (0%)22/34 (64.7%)
Netupitant 4 mg/kg Plus Palonosetron0/32 (0%)3/32 (9.4%)22/32 (68.8%)
Most frequent serious events
Most frequent serious events
EventNetupitant 1.33 mg/kg Plus PalonosetronNetupitant 4 mg/kg Plus Palonosetron
Febrile neutropeniaBlood and lymphatic system disorders0/342/32
StomatitisGastrointestinal disorders0/341/32
Neutropenic sepsisInfections and infestations0/341/32
Urinary tract infectionInfections and infestations0/341/32
Most frequent other events
Showing 10 of 16
Most frequent other events
EventNetupitant 1.33 mg/kg Plus PalonosetronNetupitant 4 mg/kg Plus Palonosetron
ThrombocytopeniaBlood and lymphatic system disorders10/346/32
AnaemiaBlood and lymphatic system disorders9/347/32
LeukopeniaBlood and lymphatic system disorders8/344/32
NeutropeniaBlood and lymphatic system disorders3/346/32
StomatitisGastrointestinal disorders2/345/32
PyrexiaGeneral disorders1/345/32
Febrile neutropeniaBlood and lymphatic system disorders2/343/32
VomitingGastrointestinal disorders2/343/32
Alanine aminotransferase increasedInvestigations3/341/32
NauseaGastrointestinal disorders1/342/32

Baseline characteristics

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
Age, Continuous(years)Netupitant 1.33 mg/kg Plus PalonosetronNetupitant 4 mg/kg Plus PalonosetronTotal
Mean6.6 ± 6.295.6 ± 5.466.1 ± 5.88
Age, Customized
Age, Customized(Participants)Netupitant 1.33 mg/kg Plus PalonosetronNetupitant 4 mg/kg Plus PalonosetronTotal
3 to <6 months325
6 to <12 months459
1 to <2 years347
2 to <5 years6612
5 to <12 years8816
12 to <18 years9716
1 to <3 months101
Sex: Female, Male
Sex: Female, Male(Participants)Netupitant 1.33 mg/kg Plus PalonosetronNetupitant 4 mg/kg Plus PalonosetronTotal
Female131427
Male211839
Race (NIH/OMB)
Race (NIH/OMB)(Participants)Netupitant 1.33 mg/kg Plus PalonosetronNetupitant 4 mg/kg Plus PalonosetronTotal
American Indian or Alaska Native000
Asian011
Native Hawaiian or Other Pacific Islander000
Black or African American000
White343165
More than one race000
Unknown or Not Reported000
08

Study locations

17 sites
  • Nemours/A.I. duPont Hospital for Children
    Wilmington, Delaware 19803, United States
  • Nemours Children's Clinic
    Jacksonville, Florida 32207, United States
  • Nemours Children's Hospital - Orlando
    Orlando, Florida 32827, United States
  • Maine Medical Center - Cancer Medicine and Blood Disorders - Scarborough
    Scarborough, Maine 04074, United States
  • Medical University of South Carolina
    Charleston, South Carolina 29425, United States
  • Chelyabinsk Regional Children's Clinical Hospital
    Chelyabinsk, Russian Federation
  • Children's Territorial Clinical Hospital
    Krasnodar, Russian Federation
  • Dmitry Rogachev National Scientific and Practical Center for Pediatric Hematology, Oncology and Immunology
    Moscow, Russian Federation
  • City Clinical Hospital #31
    St. Petersburg, Russian Federation
  • First I.P. Pavlov State Medical University of St. Petersburg
    St. Petersburg, Russian Federation
  • Voronezh Regional Children's Cinical Hospital #1
    Voronezh, 394024, Russian Federation
  • Regional Children's Clinical Hospital #1
    Yekaterinburg, Russian Federation
  • University Children's Hospital, Center for Pediatrics, Department of Hematology and Oncology
    Belgrade, Serbia
  • Clinical Center Nis, Clinic of Pediatric Internal Diseases
    Nis, Serbia
  • Dnipropetrovsk Regional Children's Clinical Hospital
    Dnipro, 49100, Ukraine
  • National Institute of Cancer, Research Department of Pediatric Oncology
    Kyiv, Ukraine
  • West Ukrainian Specialized Children's Medical Center, Department of Pediatric Surgery
    Lviv, Ukraine
09

References and documents

Study documents

PDFs hosted by the registry, ClinicalTrials.gov.

Individual participant data

Plan to share: No

10

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 25, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
11

Registry details

Key details

Study ID
NCT03204279
Responsible party
Sponsor
First posted
Jul 2, 2017
Start date
Aug 31, 2017
Primary completion
Sep 30, 2019
Completion
Sep 30, 2019
Results posted
Dec 7, 2020
Last update
Jun 25, 2024

Oversight

Data monitoring committee
Yes
FDA-regulated drug
Yes
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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Discussion

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Studies of the drugs tested here: Netupitant · Palonosetron

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