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ALK+ Non-Small-Cell Lung CarcinomaLOREANCT06487078

Analysis of the Effectiveness and Safety of Lorlatinib in Untreated ALK-Positive NSCLC Patients in a French Real-World Context

A study testing Lorlatinib in people with ALK+ Non-Small-Cell Lung Carcinoma, run by Pfizer at 32 sites in France.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record

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Trial summary

Analysis of the Effectiveness and Safety of Lorlatinib in Untreated ALK-Positive NSCLC Patients in a French Real-World context Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
ALK+ Non-Small-Cell Lung Carcinoma
What is being tested?
Lorlatinib
Type of treatment
Pill or oral medicine
Could I receive a placebo?
No, everyone receives an active treatment
How many people
90 participants
Where
32 sitesFrance
Study dates
20 Jan 2025to 30 Nov 2028
Phase
Interventional

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Inclusion Criteria: Participants are eligible to be included in the study only if all the following criteria apply:

  • Patients (male or female) 18 years of age or older at age inclusion
  • Patients with histologically or cytologically confirmed diagnosis of locally advanced or metastatic (TNM 8th classification) ALK-positive NSCLC (IHC 3+/FISH positive/transcriptomic method)
  • Complete radiological evaluation has to be performed before the start of lorlatinib by contrast enhanced CT-scan of thorax and upper abdomen and brain MRI, as per routine care
  • Patients with ECOG performance status grade 0, 1, or 2

Exclusion Criteria: Participants are excluded from the study if any of the following criteria Apply

  • Evidence of active malignancy within the last 2 years prior to inclusion (other than NSCLC, non-melanoma skin cancer, cervical in situ cancer, papillary thyroid cancer, lobular carcinoma in situ/ductal carcinoma in situ (LCIS/DCIS) of the breast, or localized prostate cancer).
  • Patients who have previously received adjuvant ALK TKI therapy (unless metastatic relapse occurs more than one year after completion of adjuvant therapy).
  • Patients who have previously received systemic NSCLC therapy in metastatic condition.
  • Patients using any of the following food or drugs within 12 days prior to the first dose of lorlatinib:
  • known strong CYP3A inhibitors
  • known strong CYP3A inducers
  • known P gp substrates with a narrow therapeutic index
  • Patients with any medical or psychiatric condition, or that may, in the investigator's judgment, increase the risk of study participation or make the participant inappropriate for the study.
  • Positive pregnancy test for females of childbearing potential.
  • Breastfeeding and childbearing potential female unwilling/unable to use a highly effective contraception method for the study duration and for at least 35 days after the last dose of lorlatinib
  • Fertile male patients unwilling/unable to use a highly effective method of contraception for the duration of the study and for at least 97 days after the last dose of lorlatinib.
  • Patients participating in another clinical study, unless it is an observational (non-interventional) clinical study or during the follow-up period of an interventional study.
  • Patients deprived of their liberty, under protective custody or guardianship or unable to provide signed consent.
  • Patients not affiliated to the French social security system.
  • Patients opposed to the collection of their data.
  • Patients willing and able to comply with the protocol for the duration of the study including undergoing treatment, scheduled visits and examinations including follow-up.
  • Patients judged inapt to respond to the questions required for the study due to linguistical, psychological, social, or geographical reasons.
  • Investigator site staff directly involved in the conduct of the study and their family members, site staff otherwise supervised by the investigator, and sponsor and sponsor delegate employees directly involved in the conduct of the study and their family members.

Trial locations and contacts

32 sites in 1 country. Contact the study team or a site near you to ask about taking part.

32 sites in 1 country

France32 sites, 32 recruiting
  • Centre Hospitalier du Pays d AIX

    Aix-en-Provence, 13100

    Recruiting
  • CH ALBI

    Albi, 81000

    Recruiting
  • Chu Amiens Sud

    Amiens, 80000

    Recruiting
  • Ch Avignon

    Avignon, 84000

    Not yet recruiting
  • Polyclinique Bordeaux Nord Aquitaine

    Bordeaux, 30072

    Not yet recruiting
  • Institut Bergonie

    Bordeaux, 33076

    Not yet recruiting
  • Hopital Morvan

    Brest, 29000

    Not yet recruiting
  • CHIC

    Créteil, 94010

    Recruiting
  • Clcc Georges Francois Leclerc

    Dijon, 21000

    Recruiting
  • Hopital de Villefranche Sur Saone

    Gleizé, 69400

    Not yet recruiting
  • Chu Limoges

    Limoges, 87042

    Recruiting
  • Centre Leon Berard

    Lyon, 69373

    Not yet recruiting
  • Hopital Robert Schuman de Vantoux

    Metz, 57070

    Recruiting
  • CHU Nantes

    Nantes, 44093

    Recruiting
  • Institut Curie

    Paris, Paris, 75005

    Recruiting
  • Hopital Cochin

    Paris, 75014

    Not yet recruiting
  • Hopital Europeen Georges Pompidou

    Paris, 75015

    Recruiting
  • Hopital Saint Joseph

    Paris, 75674

    Recruiting
  • Centre Hospitalier Francois Mitterand

    Pau, 64046

    Recruiting
  • Ch Annecy Genevois

    Pringy, 74374

    Recruiting
  • Ch Cornouaille

    Quimper, 29107

    Recruiting
  • Institut Godinot

    Reims, 51056

    Recruiting
  • Hopital Pontchaillou

    Rennes, 35033

    Recruiting
  • Hopital Foch

    Suresnes, 92151

    Recruiting
  • Chits Ch Sainte Musse

    Toulon, 83000

    Not yet recruiting
  • CHU de Toulouse - Hopital Larrey

    Toulouse, Haute-garonne, 31059

    Recruiting
  • CHRU Bretonneau

    Tours, 37000

    Recruiting
  • Ch Troyes

    Troyes, 10003

    Recruiting
  • Hopital de Rangueil

    TSA 50032 Toulouse, 31059

    Recruiting
  • Clinique Teissier

    Valenciennes, 59300

    Recruiting
  • Chru de Nancy-Hopital Brabois

    Vandœuvre-lès-Nancy, 54500

    Not yet recruiting
  • CHBA

    Vannes, 56017

    Recruiting

Other trials in France

About this study

Official title: LOREA : ANALYSIS OF THE EFFECTIVENESS AND SAFETY OF LORLATINIB IN UNTREATED ALK-POSITIVE NSCLC PATIENTS IN A FRENCH NON INTERVENTIONAL STUDY

Analysis of the Effectiveness and Safety of Lorlatinib in Untreated ALK-Positive NSCLC Patients in a French Real-World context

Being tested
Lorlatinib

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • LorlatinibDrug

    Also called PF-06463922

    ALK-positive NSCL treatment

Study groups in NCT06487078
Study groupRoleWhat they receive
LorlatinibExperimentalLorlatinib single agent, 100 mg (4 x 25 mg) oral tables, QD, continuously
Receives: Drug: Lorlatinib

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Progression-Free Survival (PFS)

    Time from inclusion to date of disease progression or death of any cause whichever occurs first.

    Measured: From time of Study Start up to 25 months

Secondary outcomes (17)
  1. Overall Survival (OS)

    Time from inclusion to date of death from any cause.

    Measured: From time of Study Start up to 25 months

  2. Objective Response Rate (ORR)

    proportion of patients with a Complete Response (CR) or Partial Response (PR) as a best response during the lorlatinib treatment. Responses to treatment will be defined according to investigator

    Measured: From time of Study Start up to 24 months

  3. Duration of Response (DR)

    time between the first documentation of objective response and the first documentation of disease progression or death from any cause whichever occurred first, for participants with a confirmed objective response of CR or PR.

    Measured: From time of Study Start up to 24 months

  4. Intracranial Objective Response Rate (IC-ORR)

    proportion of patients with intracranial objective response of complete response (CR) or partial response (PR) as a best response in the subset of patients with at least 1 intracranial lesion assessed by investigator.

    Measured: From time of Study Start up to 24 months

  5. Intracranial Time to Progression (IC-TTP)

    Time from inclusion to the date of the first documentation of disease progression of intracranial disease, based on either new brain metastases or progression of existing brain metastases.

    Measured: From time of Study Start up to 24 months

  6. Intracranial Duration of Response (IC-DR)

    time from the first documentation of intracranial OR to the first documentation of intracranial progressive disease (PD) or death due to any cause, whichever occurred first for participants with a confirmed objective response of CR or PR assessed by investigator.

    Measured: From time of Study Start up to 24 months

  7. Duration of Treatment (DT)

    Time between inclusion and last dose of lorlatinib.

    Measured: From time of Study Start up to 25 months

  8. Proportion of patients with extracranial progression and sites of progression

    Based on Investigator's Assessment

    Measured: From time of Study Start up to 24 months

  9. Time to Treatment Failure (TTF)

    Time from date of treatment initiation to date of discontinuation of treatment for any reason, including progression of disease, treatment toxicity, and death from any cause whichever occurs first.

    Measured: From time of Study Start up to 24 months

  10. Adverse Event (AE) as graded by NCI CTCAE v5)

    Frequency of patients experiencing treatment-emergent AEs (TEAEs)

    Measured: From time of Study Start up to 25 months

  11. Number of Participants With Treatment-Emergent Adverse Events (AEs; Treatment-Related

    Treatment-emergent AEs were those with initial onset or that worsen in severity after the first dose of study medication. Treatment-related AEs were determined by investigators.

    Measured: From time of Study Start up to 25 months

  12. Proportion of patients considered observant to treatment assessed by the compliance questionnaire.

    Self-administered questionnaire that provides a measure of compliance

    Measured: At the start of cycle (each cyle is 28 days) Cycle2Day1, Cycle3Day1, Cycle4Day1 and then every 3 months - as long as 48 months

  13. Proportion of patients experiencing a 10-points change from baseline in total score for the EORTC QLQ-C30

    evaluate Health-related Quality of life (HRQoL) of ALK- positive locally advanced or metastatic NSCLC patients treated with lorlatinib in first-line using the EORTC QLQ-C30 questionnaires

    Measured: At inclusion, At the start of Cycle (each cycle is 28 days) Cycle2Day1, Cycle3Day1, Cycle4Day1 and every 3 months until the first year and then every 6 months - as long as 48 months

  14. Proportion of patients experiencing a 10-points change from baseline in total score for the EORT QLQ-LC13.

    Evaluate Health-related Quality of life (HRQoL) of ALK- positive locally advanced or metastatic NSCLC patients treated with lorlatinib in first-line using the EORTC QLQ -LC13 questionnaires

    Measured: At inclusion, At the start of Cycle (each cycle is 28 days) Cycle2Day1, Cycle3Day1, Cycle4Day1 and every 3 months until the first year and then every 6 months - as long as 48 months

  15. Patient Reported Outcome-informed CNS symptomatic toxicity:

    frequency, severity and/or interference with daily activities, amount, presence/absence according to PRO-CTCAE questionnaires for mood (anxious/discouraged/sad), and attention/memory items (concentration/memory).

    Measured: At inclusion, At the start of cycle (each cycle is 28 days) Cycle1Day15, Cycle2Day1, Cycle3Day1, Cycle4Day1 and every 3 months until the first year and then every 6 months - as long as 48 months

  16. Proportion of patients experiencing grade III toxicities or progression and having an over- or under-exposure to lorlatinib.

    At each time point, a blood sample to provide plasma for determination of the plasma concentrations of lorlatinib.

    Measured: At baseline, at start of Cycle1Day15 (each cycle is 28 days), Month 3, Month 9 and every 6 months through the end of treatment, at time of first grade III of hyperlipidaemia and CNS toxicity onset, and at progression - as long as 48 months

  17. Proportion of patients experiencing each kind of identified lorlatinib resistance mechanisms

    Plasma samples collected at baseline and end of treatment, analyzed by next-generation sequencing

    Measured: At baseline and at the date of first documented progression (as long as 48 months)

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted5 Jul 2024
  2. Study start20 Jan 2025
  3. Primary completion30 Nov 2028 (estimated)
  4. Study completion30 Nov 2028 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
90 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06487078
Sponsor's protocol ID
B7461051
Other IDs
LOREA
Acronym
LOREA
Status last verified
Oct 2026
First submitted
5 Jun 2024
Last updated
23 Oct 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: Pfizer will provide access to individual de-identified participant data and related study documents (e.g. protocol, Statistical Analysis Plan (SAP), Clinical Study Report (CSR)) upon request from qualified researchers, and subject to certain criteria, conditions, and exceptions. Further details on Pfizer's data sharing criteria and process for requesting access can be found at: https://www.pfizer.com/science/clinical\_trials/trial\_data\_and\_results/data\_requests.

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