Asciminib as Single Agent or in Combination With Nilotinib in the 1st-line Treatment of BCR-ABL1+ Chronic Myeloid Leukemia: a Randomized GIMEMA-GELMC Phase II Study PEARL Study: PotEntial of Asciminib in the eaRly Treatment of CML

Status: Recruiting
Location: See all (11) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

A phase 2, interventional, randomized unblinded study will be conducted in newly diagnosed CP CML patients, to investigate the efficacy and the safety of asciminib at a dose of 80 mg QD as single agent (arm A) or 40 mg BID in combination with nilotinib 300 mg BID (arm B). All patients in both arm A and arm B will be treated for a minimum of 2 years (core phase). If they will have achieved a DMR (MR4), or if it will be in the interest of the patient, the treatment will be continued. During the consolidation phase (2 years) asciminib will be continued at the same dose in both arms; in the combination arm the nilotinib dose will be reduced to 300 mg daily. The patients maintaining a stable MR4 up to the end of the fourth year will discontinue the treatment (TFR phase). The rate of TFR at 5 year (1 year after discontinuation) will be evaluated.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Cytogenetic and molecular confirmed diagnosis of Ph+ and BCR::ABL1+ CML

• Age ≥ 18 years

• Early chronic phase, less than 3 months from diagnosis

• Evidence at the time of study entry of typical BCR::ABL1 RNA transcripts e13a2 or e14a2 (b2a2 or b3a2), which are required for BCR::ABL1 international scale reporting

• Prior treatment with any TKI for 30 days or less; prior treatment with hydroxyurea or anagrelide is allowed

• ECOG performance status of 0, 1 or 2

• Adequate end organ function as defined by Total bilirubin ≤ 1.5 x ULN except for patients with Gilbert's syndrome who may only be included if total bilirubin ≤ 3.0 x ULN or direct bilirubin ≤ 1.5 x ULN Aspartate transaminase (AST) ≤ 3.0 x ULN Alanine transaminase (ALT) ≤ 3.0 x ULN Serum amylase ≤ ULN Serum lipase ≤ ULN Alkaline phosphatase ≤ 2.5 x ULN, unless considered tumor related Creatinine clearance \> 50 ml/min using Cockcroft-Gault formula

• Signed written informed consent according to ICH/EU/GCP and national local laws prior to any study procedure

• An effective form of contraception with their sexual partners from enrolment through 30 days after the end of treatment

Locations
Other Locations
Spain
Hospital del Mar (Barcelona)
RECRUITING
Barcelona
Hospital Universitario Basurto
RECRUITING
Bilbao
Institut Català d'Oncologia Girona
RECRUITING
Girona
Hospital Virgen de las Nieves
RECRUITING
Granada
Hospital Universitario de Gran Canaria Dr. Negrín
RECRUITING
Las Palmas De Gran Canaria
Hospital Gral U. Gregorio Marañón
RECRUITING
Madrid
Hospital Universitario 12 de Octubre
RECRUITING
Madrid
Hospital Universitario La Paz
RECRUITING
Madrid
Hospital Clínico Universitario Virgen de la Arrixaca
RECRUITING
Murcia
Complejo Asistencial Universitario de Salamanca
RECRUITING
Salamanca
Hospital Universitario La Fe Valencia
RECRUITING
Valencia
Contact Information
Primary
Paola Fazi
p.fazi@gimema.it
0670390528
Backup
Enrico Crea
e.crea@gimema.it
0670390514
Time Frame
Start Date: 2025-06-26
Estimated Completion Date: 2032-06
Participants
Target number of participants: 160
Treatments
Experimental: Asciminib single agent
Core phase (2 years): asciminib 80 mg QD will be given as single-agent.~Consolidation phase (2 years): If patients will have achieved a DMR (MR4), or if it will be in their interest, the treatment will be continued with asciminib 80 mg QD.~Treatment free remission phase (1 year): patients maintaining a stable MR4 up to the end of the fourth year will discontinue the treatment
Experimental: Asciminib plus nilotinib
Core phase (2 years): asciminib 80 mg QD will be started, then after 90 days asciminib will be given 40 mg BID and nilotinib 300 mg BID, or 300 mg OAD according to the presence/absence of asciminib adverse events, will be added-on.~Consolidation phase (2 years): If patients will have achieved a DMR (MR4), or if it will be in their interest, the treatment will be continued with asciminib 40 mg BID and nilotinib reduced to 300 mg daily.~Treatment free remission phase (1 year): patients maintaining a stable MR4 up to the end of the fourth year will discontinue the treatment
Sponsors
Leads: Gruppo Italiano Malattie EMatologiche dell'Adulto
Collaborators: Grupo Español de Leucemia Mieloide Crónica

This content was sourced from clinicaltrials.gov

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