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Idelalisib With Rituximab, Ifosfamide, Carboplatin, Etoposide (RICE) in Children and Adolescents

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ClinicalTrials.gov Identifier: NCT03349346
Recruitment Status : Withdrawn (The European Medical Agency granted a Paediatric Investigational Product-specific waiver on the grounds that idelalisib is likely to be unsafe in paediatrics)
First Posted : November 21, 2017
Last Update Posted : December 11, 2018
Sponsor:
Information provided by (Responsible Party):
Gilead Sciences

Brief Summary:
The primary objectives of this study are to evaluate safety, tolerability, pharmacokinetics (PK) and preliminary efficacy of idelalisib; and to establish recommended phase 2 doses (RP2D) of idelalisib in combination with rituximab, ifosfamide, carboplatin, etoposide (RICE) in children and adolescents with relapsed or refractory diffuse large B-cell lymphoma (DLBCL) or mediastinal B-cell lymphoma (MBCL)

Condition or disease Intervention/treatment Phase
Diffuse Large B-Cell Lymphoma Mediastinal B-cell Lymphoma Drug: Idelalisib Drug: Rituximab Drug: Ifosfamide Drug: Carboplatin Drug: Etoposide Phase 1

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 0 participants
Allocation: Non-Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Phase 1b Trial Evaluating Idelalisib in Children and Adolescents With Relapsed or Refractory Diffuse Large B-cell Lymphoma or Mediastinal B-cell Lymphoma in Combination With RICE
Estimated Study Start Date : June 2019
Estimated Primary Completion Date : February 2021
Estimated Study Completion Date : February 2026


Arm Intervention/treatment
Experimental: Cohort 1- Participants 12 to less than 18 years of age

Participants will receive idelalisib monotherapy (from day 1 to day 21), followed by combination therapy with RICE. Upon enrollment, participants will be assigned to one of the 3 dose levels during idelalisib monotherapy (Dose level 1 = 55 mg/m^2 twice daily (BID), Dose level 2 = 85 mg/m^2 BID, Dose level 3 = 125 mg/m^2 BID) administered as 50 mg, 100 mg or 150 mg tablets as appropriate, or as 10 mg dispersible tablets for oral suspension for participants who cannot swallow tablets.

  • Day 1: single dose of idelalisib
  • Day 2 up to Day 21: initiate and continue idelalisib BID dosing
  • Day 22 for up to 12 months: idelalisib twice per day in combination with RICE. Cycles of RICE will be administered over 5 days every 3 weeks (Day 1: rituximab; Day 3: rituximab, ifosfamide, carboplatin, etoposide; Days 4 and 5: ifosfamide, etoposide) starting day 22 (or earlier if there is evidence of clinical progression while on idelalisib monotherapy) for up to 12 months.
Drug: Idelalisib
Tablet (s) or dispersible tablets for suspension administered orally twice daily
Other Name: Zydelig®

Drug: Rituximab
375 mg/m^2 administered intravenously

Drug: Ifosfamide
3 mg/m^2 administered intravenously

Drug: Carboplatin
635 mg/m^2 administered intravenously

Drug: Etoposide
100 mg/m^2 administered intravenously

Experimental: Cohort 2- Participants 1 to less than 12 years of age

Participants will receive one of the 3 doses of idelalisib monotherapy (from day 1 to day 21) followed by combination therapy with RICE. Idelalisib will be administered as as 50 mg, 100 mg or 150 mg tablets as appropriate, or as 10 mg dispersible tablets for oral suspension for participants who cannot swallow tablets. Participants will will be enrolled at dose level 1 once tolerability is demonstrated in the older cohort (Cohort 1). Thereafter, both age cohorts will be dose escalated independently.

  • Day 1: single dose of idelalisib
  • Day 2 up to Day 21: initiate and continue idelalisib BID
  • Day 22 for up to 12 months: idelalisib twice per day in combination with RICE. Cycles of RICE will be administered over 5 days every 3 weeks (Day 1: rituximab; Day 3: rituximab, ifosfamide, carboplatin, etoposide; Days 4 and 5: ifosfamide, etoposide) starting day 22 (or earlier if there is evidence of clinical progression while on idelalisib monotherapy) for up to 12 months.
Drug: Idelalisib
Tablet (s) or dispersible tablets for suspension administered orally twice daily
Other Name: Zydelig®

Drug: Rituximab
375 mg/m^2 administered intravenously

Drug: Ifosfamide
3 mg/m^2 administered intravenously

Drug: Carboplatin
635 mg/m^2 administered intravenously

Drug: Etoposide
100 mg/m^2 administered intravenously




Primary Outcome Measures :
  1. Incidence Rate of Dose Limiting Toxicities (DLTs) [ Time Frame: Up to Day 21 ]
    DLTs refer to toxicities experienced during the first 21 days of study treatment that have been judged to be clinically significant and related to study treatment.

  2. Proportion of Participants Experiencing Adverse Events (AEs) [ Time Frame: Up to 12 months ]
  3. Proportion of Participants Experiencing Serious Adverse Events (SAEs) [ Time Frame: Up to 12 months ]
  4. Proportion of Participants Experiencing Adverse Events (AEs) Leading to Idelalisib Interruption, Idelalisib Dose Reduction, Premature Discontinuation of Idelalisib, or Death [ Time Frame: Up to 12 months ]

Secondary Outcome Measures :
  1. Rate of Grade ≥ 3 Transaminase Elevations Based on Laboratory Findings [ Time Frame: Up to 12 months ]
  2. Overall Response Rate (ORR) [ Time Frame: Up to 12 months ]
    Overall response rate (ORR) is defined as the proportion of participants who achieve a best response of Complete Response (CR) or Partial Response (PR) after the first dose of idelalisib (either as a result of monotherapy or in combination with RICE chemoimmunotherapy). The screening imaging study will serve as the reference for ORR.

  3. Overall Survival (OS) [ Time Frame: Up to 5 years ]
    Overall Survival (OS) is defined as the interval from the first dose date of idelalisib to death from any cause.

  4. Progression-Free Survival (PFS) [ Time Frame: Up to 12 months ]
    Progression-Free Survival (PFS) is defined as the interval from the start date of RICE to the earlier of the first documentation of disease progression or death from any cause. Computed tomography/ magnetic resonance imaging (CT/MRI) scan at the conclusion of idelalisib monotherapy will serve as the reference for progression.

  5. Pharmacokinetic Parameter: Cmax of Idelalisib [ Time Frame: Predose and up to 24 hours postdose on Day 1 and Cycle 1, Day 5 of idelalisib + RICE combination therapy ]
    Cmax is defined as the maximum observed concentration of drug.

  6. Pharmacokinetic Parameter: Cmax of GS-563117 [ Time Frame: Predose and up to 24 hours postdose on Day 1 and Cycle 1, Day 5 of idelalisib + RICE combination therapy ]
    GS-563117 is the metabolite of idelalisib. Cmax is defined as the maximum observed concentration of drug.

  7. Pharmacokinetic Parameter: Ctrough of Idelalisib [ Time Frame: Predose and up to 24 hours postdose on Day 1 and Cycle 1, Day 5 of idelalisib + RICE combination therapy ]
    Ctrough is defined as the plasma concentration at the end of the dosing interval.

  8. Pharmacokinetic Parameter: Ctrough of GS-563117 [ Time Frame: Predose and up to 24 hours postdose on Day 1 and Cycle 1, Day 5 of idelalisib + RICE combination therapy ]
    Ctrough is defined as the plasma concentration at the end of the dosing interval.

  9. Pharmacokinetic Parameter: Area Under the Concentration-Time Curve (AUC) of Idelalisib [ Time Frame: Predose and up to 24 hours postdose on Day 1 and Cycle 1, Day 5 of idelalisib + RICE combination therapy ]
    AUC is defined as the plasma concentration at the end of the dosing interval.

  10. Pharmacokinetic Parameter: Area Under the Concentration-Time Curve (AUC) of GS-563117 [ Time Frame: Predose and up to 24 hours postdose on Day 1 and Cycle 1, Day 5 of idelalisib + RICE combination therapy ]
    AUC is defined as the plasma concentration at the end of the dosing interval.

  11. Levels of Optional Exploratory Biomarkers on Bone Marrow Samples (eg pAKT, pS6 ribosomal protein) and plasma cytokines [ Time Frame: Baseline and Day 21 ]
  12. Acceptability and Palatability of Idelalisib 10-mg Dispersible Tablet [ Time Frame: Day 1 of idelalisib monotherapy and at Day 1, Cycle 1 of idelalisib in combination with RICE chemoimmunotherapy ]
    For participants who cannot swallow a whole tablet, the investigator will ask if the tablet administered as a suspension is palatable and will observe if the participant is able to swallow the dosage form. The acceptability and palatability of idelalisib dispersible tablets administered as an oral suspension (for participants unable to swallow the tablet) will be evaluated by a questionnaire administered to the participant and/or the parent/legal guardian.



Information from the National Library of Medicine

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Ages Eligible for Study:   1 Year to 18 Years   (Child, Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Key Inclusion Criteria:

  • Histologically confirmed diagnosis of DLBCL or MBCL established by the World Health Organization (WHO) 2008 classification of tumors of hematopoietic and lymphoid tissues
  • Relapsed or refractory disease
  • Measurable or evaluable disease based on imaging or bone marrow examination
  • Karnofsky ≥ 60% for participants > 16 years of age or Lansky ≥ 60 for participants ≤ 16 years of age. Participants who are unable to walk because of paralysis, but who are up in a wheelchair, will be considered ambulatory for the purpose of assessing the performance score.
  • A negative serum pregnancy test is required for females of child bearing potential.
  • Participants of child bearing potential who engage in heterosexual intercourse must agree to use protocol specified method(s) of contraception .
  • Lactating females must agree to discontinue nursing before idelalisib is administered
  • Adequate bone marrow function as defined in the protocol
  • Adequate renal function as defined in the protocol

Key Exclusion Criteria:

  • Prior ifosfamide, carboplatin, etoposide (ICE) therapy, with or without an anti-CD20 antibody, or history of hypersensitivity to any components of RICE
  • Known active central nervous system or leptomeningeal lymphoma or within 4 weeks from the last intrathecal therapy prior to the required diagnostic lumbar puncture (LP) for this study
  • Disease progression within 6 months from last anti-CD20 therapy
  • Ongoing toxicity from prior cytotoxic therapy (last dose at least 3 weeks prior to study entry)
  • Less than 4 half-lives from the last dose of previous targeted therapy and ongoing acute toxicity of prior targeted therapy
  • Active infection with human immunodeficiency virus (HIV), cytomegalovirus (CMV), hepatitis B virus (HBV), or hepatitis C virus (HCV) based on screening serology and polymerase chain reaction (PCR) results
  • Evidence of systemic bacterial, fungal, or viral infection at the time of treatment start (Day 1)
  • Ongoing or history of drug-induced pneumonitis
  • Ongoing or history of inflammatory bowel disease
  • Pregnancy or breastfeeding
  • Currently receiving other anti-cancer or other investigational drug
  • Prior solid organ transplantation
  • Prior allogeneic stem cell transplantation within 60 days or active acute graft versus host disease (GVHD) Grade 3 or higher
  • Known hypersensitivity to idelalisib, the metabolites, or formulation excipients
  • Any other clinical condition or prior therapy that, in the opinion of the Investigator, would make the participant unsuitable for the study or unable to comply with the study requirements

NOTE: Other protocol defined Inclusion/ Exclusion criteria may apply.


Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03349346


Locations
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France
Centre Hospitalier Régional Universitaire de Lille
Lille, France, 59000
Italy
Istituto Giannina Gaslini
Genova, Italy, 16147
Ospedale Pediatrico Bambino Gesu
Roma, Italy, 00165
Infantile Regina Margherita Hospital
Torino, Italy, 10126
Poland
Uniwersytecki Szpital Kliniczny im. Jana Mikulicza-Radeckiego we Wroclawiu
Wrocław, Poland, 50-556
Spain
Hospital Vall d´Hebrón
Barcelona, Spain, 08035
Hospital Universitario HM Monteprincipe
Madrid, Spain, 28660
Sponsors and Collaborators
Gilead Sciences
Investigators
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Study Director: Gilead Study Director Gilead Sciences

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Responsible Party: Gilead Sciences
ClinicalTrials.gov Identifier: NCT03349346     History of Changes
Other Study ID Numbers: GS-US-313-1090
2017-001468-39 ( EudraCT Number )
First Posted: November 21, 2017    Key Record Dates
Last Update Posted: December 11, 2018
Last Verified: December 2018

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Studies a U.S. FDA-regulated Drug Product: Yes
Studies a U.S. FDA-regulated Device Product: No
Product Manufactured in and Exported from the U.S.: Yes

Additional relevant MeSH terms:
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Lymphoma
Lymphoma, B-Cell
Lymphoma, Large B-Cell, Diffuse
Neoplasms by Histologic Type
Neoplasms
Lymphoproliferative Disorders
Lymphatic Diseases
Immunoproliferative Disorders
Immune System Diseases
Lymphoma, Non-Hodgkin
Carboplatin
Rituximab
Etoposide
Etoposide phosphate
Ifosfamide
Isophosphamide mustard
Idelalisib
Antineoplastic Agents
Antineoplastic Agents, Immunological
Immunologic Factors
Physiological Effects of Drugs
Antirheumatic Agents
Antineoplastic Agents, Phytogenic
Topoisomerase II Inhibitors
Topoisomerase Inhibitors
Enzyme Inhibitors
Molecular Mechanisms of Pharmacological Action
Antineoplastic Agents, Alkylating
Alkylating Agents