Study of Lurbinectedin Monotherapy in Pediatric and Young Adult Participants With Relapsed/Refractory Ewing Sarcoma

Trial statusRecruiting
Trial phasePhase 1, Phase 2
Trial typeInterventional
Biological sexAll
Age2-30
SponsorJazz Pharmaceuticals

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 volunteers

Qualifiers

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

Design model

Sequential

Treatments tested in this trial

  • Lurbinectedin

    Drug

    Administered as intravenous (IV) infusion once every 3 weeks (Q3W)

Treatment groups

60 Participants
are divided into 3 treatment groups
Group A: Phase 1 Part 1: Dose SelectionExperimental treatment 1 intervention
Group B: Phase 1 Part 2: RP2DExperimental treatment 1 intervention
Group C: Phase 2Experimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Phase 1: Number of Participants Experiencing Dose-limiting Toxicities (DLTs)

Time frame
From the first dose through end of Cycle 1 (21 days).
2

Phase 1: Number of Participants Experiencing Serious Adverse Events (SAEs) and Treatment Emergent Adverse Events (TEAEs)

Time frame
Post-baseline (Day 1) up to approximately 31 months.
3

Phase 1: Number of Participants With Dose Modifications

Time frame
Post-baseline (Day 1) up to approximately 31 months.
4

Phase 1: Number of Participants Who Discontinued Study Intervention Due to TEAEs

Time frame
Post-baseline (Day 1) up to approximately 31 months.

Secondary outcomes

1

Phase 1: Plasma Concentration of Lurbinectedin

Time frame
Day 1: Predose up to approximately 168 hours postdose; Days 16, 31, 46: Predose up to approximately 5 minutes postdose.
2

Phase 1: Objective Response Rate (ORR) Based on Investigator Assessment (IA)

Time frame
Day -28 up to a total of 31 months postdose.
3

Phase 1: Progression-Free Survival (PFS) Based on Investigator Assessment (IA)

Time frame
Day -28 up to a total of 31 months postdose.
4

Phase 1: Duration of Response (DOR) in Participants with Confirmed Complete Response (CR) or Partial Response (PR)

Time frame
Day -28 up to a total of 31 months postdose.

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Jazz Pharmaceuticals

Lead sponsor

Jazz Pharmaceuticals Ireland Limited

Collaborator