Clinical Trials Logo

Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03810872
Other study ID # Precision 2 - 1200.264
Secondary ID
Status Recruiting
Phase Phase 2
First received
Last updated
Start date June 21, 2017
Est. completion date December 2022

Study information

Verified date January 2019
Source AZ-VUB
Contact Lore Decoster, Dr
Phone +32 2 477 64 15
Email lore.decoster@uzbrussel.be
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Objective(s):To investigate the efficacy and safety of afatinib in EGFR, HER 2 and HER3 mutated cancers, regardless of cancer type, excluding EGFR mutated non-small cell lung cancer.

Methodology:Open label, genomic driven trial (basket trial)

No. of patients total entered:Optimal Simon two stage design for the three genetic driven cohorts: 10 patients will be enrolled per cancer type in the first stage and an additional 19 in the second stage (maximum total 87 patients)

Indication : cancers harbouring an EGFR mutation(excluding non-squamous non- small cell lung cancer, a registered indication), a HER2 mutation or a HER3 mutation

Test product(s) : Afatinib At progression paclitaxel will be added for those patients that have no contra-indications

dose: Starting dose of afatinib at 40 mg/day. Dose increase to 50 mg in the absence of adverse events. Stepwise dose reduction to 30,20, 10 mg/day according to drug-related adverse events.

At progression, addition of paclitaxel 80 mg/m2 weekly 3w/4 to afatinib 40 mg/day .

mode of admin. : Oral for afatinib Intravenous for paclitaxel

Duration of treatment: Continuous treatment until progression or unacceptable adverse events or withdrawal of consent.

At disease progression, add paclitaxel until progression or unacceptable adverse event or withdrawal of consent if no contra-indications.

Criteria for efficacy: Primary Endpoint:

• Response rate (CR+ PR) via RECIST v1.1

Secondary Endpoints:

- Disease control rate (CR+PR+SD)

- Progression free survival

- Overall survival

- To correlate tumor response with findings on tumor biopsies

- To investigate resistance mechanisms

- response rate (CR+ PR) determined by RECIST and progression free survival on the combination therapy of afatinib and paclitaxel

Criteria for safety: Incidence and intensity of adverse events according CTCAE v4.0


Recruitment information / eligibility

Status Recruiting
Enrollment 87
Est. completion date December 2022
Est. primary completion date December 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Women and men with locally advanced or metastatic cancers harboring either an activating EGFR mutation or a HER2 mutation or a HER3 mutation

- Failure of at least one line of standard systemic therapy

- No eligibility for other open genomic driven phase I, II or III trial available for these tumor genotypes

- ECOG performance status =2

- Patient with a life expectancy >3 months

- Patients able to provide written informed consent prior to enrollment into the clinical trial.

- Adequate organ function

Exclusion Criteria:

- Non squamous non-small cell lung cancer harbouring an EGFR mutation (registered indication)

- Chemotherapy, biological therapy or investigational agents within four weeks prior to the start of study treatment

- Known hypersensitivity to afatinib or the excipients of any of the trial drugs

- Prior treatment with afatinib

Study Design


Intervention

Drug:
Afatinib
Open label
Paclitaxel
Paclitaxel

Locations

Country Name City State
Belgium Institut Jules Bordet Brussels
Belgium Les Cliniques Universitaires St Luc Brussels
Belgium Universitaire Ziekenhuis Antwerpen Edegem
Belgium UZ Gent Gent
Belgium CHU Sart-Tilman Liège

Sponsors (1)

Lead Sponsor Collaborator
AZ-VUB

Country where clinical trial is conducted

Belgium, 

Outcome

Type Measure Description Time frame Safety issue
Primary Response rate 6 weeks
Primary Incidence and intensity of adverse events 4 weeks
Secondary Disease control rate 6 weeks
Secondary Progression free survival 6 weeks
Secondary Overall survival 6 weeks