About this trial
This study is conducted in two phases. The phase 1 portion of the study evaluates the safety, tolerability, pharmacokinetics (PK), recommended phase 2 dose (RP2D), and effectiveness of lurbinectedin monotherapy in pediatric participants with previously treated solid tumors. This is followed by the phase 2 portion, to further assess the effectiveness and safety in pediatric and young adult participants with recurrent/refractory Ewing sarcoma.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Phase 1 Part 1: participants must be ≥ 2 to < 18 years of age.
Phase 1 Part 2: participants must be ≥ 2 to ≤ 30 years of age.
Phase 2: participants must be ≥ 2 to ≤ 30 years of age.
Participant has a confirmed solid tumor
Disqualifiers
corrected QT interval (QTc) prolongation defined as a QTc ≥ 460 ms using the Bazett formula in age < 18 years and QTc ≥ 470 ms using the Bazett formula in age ≥ 18 years.
Known symptomatic Central nervous system (CNS) metastases requiring steroids. Participants with previously diagnosed CNS metastases are eligible if they have completed their treatment and have recovered from the acute effects of radiation therapy or surgery prior to enrollment, have discontinued high dose steroid treatment for these metastases for at least 2 weeks, and are neurologically stable (physiologic doses of steroids and short courses of steroids for other indications are acceptable).
Persisting toxicity related to prior therapy; however, alopecia, sensory neuropathy, hypothyroidism, and rash Grade ≤ 2 are acceptable, and other Grade ≤ 2 adverse events (AEs) not constituting a safety risk based on the investigator's judgement are acceptable.
An uncontrolled intercurrent illness including but not limited to ongoing or active infection requiring antibiotic, antifungal, or antiviral therapy, symptomatic heart failure, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements.
Trial design
Sequential
Treatments tested in this trial
Lurbinectedin
DrugAdministered as intravenous (IV) infusion once every 3 weeks (Q3W)
Treatment groups
Trial outcomes
Primary outcomes
Phase 1: Number of Participants Experiencing Dose-limiting Toxicities (DLTs)
Phase 1: Number of Participants Experiencing Serious Adverse Events (SAEs) and Treatment Emergent Adverse Events (TEAEs)
Phase 1: Number of Participants With Dose Modifications
Phase 1: Number of Participants Who Discontinued Study Intervention Due to TEAEs
Secondary outcomes
Phase 1: Plasma Concentration of Lurbinectedin
Phase 1: Objective Response Rate (ORR) Based on Investigator Assessment (IA)
Phase 1: Progression-Free Survival (PFS) Based on Investigator Assessment (IA)
Phase 1: Duration of Response (DOR) in Participants with Confirmed Complete Response (CR) or Partial Response (PR)
Sponsors and contacts
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Jazz Pharmaceuticals
Lead sponsor
Jazz Pharmaceuticals Ireland Limited
Collaborator