IP Library Granted Patent US 12,257,245
Granted Patent B2
US 12,257,245 · App. 16/534,230 · Granted Mar 25, 2025

Methods and compositions for inhibition of EGF/EGFR pathway in combination with anaplastic lymphoma kinase inhibitors

Inventors: Erik D'Hondt (Bazel, BE); Miguel Ángel Molina-Vila (Badalona, ES)
Assignee: In3Bio Ltd.
A61K31/4545A61K31/519A61K31/5377A61K31/675A61K39/001131A61K39/3955A61P35/00A61K2039/545
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Quick Facts
Patent No.
US 12,257,245
App. No.
16/534,230
Granted
Mar 25, 2025
Kind
B2
Abstract

A method of treating patients suffering from cancers driven by deregulated Human Epidermal Growth Factor Receptor (HER1/Human EGFR) comprising administering to a patient in need of such treatment a flexible and active regimen for combining Anaplastic Lymphoma Kinase Inhibitors (ALK Inhibitors) and anti-EGF antibodies for inhibition of the pathway activated by EGF-EGFR binding (mAb). The anti-EGF antibodies can be produced by active immunization or provided passively by the administration of antibodies that are anti-EGF. The method comprises ALK Inhibitors administered according to a continuous regimen based on an average daily dose in the range of 10 to 250 mg and the mAb is co-administered either actively or passively according to a dosing regimen achieving a therapeutic effective amount repeated thrice, twice or once a week, once in two weeks, once in three weeks or at least once monthly.

Claims (6)

1. A method of treating a patient suffering from a non-small cell lung cancer (NSCLC), or metastatic forms thereof, responsive to an Anaplastic Lymphoma Kinase (ALK) Inhibitor and expressing the ELM4-ALK fusion gene and a mutated form of an Epidermal Growth Factor Receptor (EGFR), comprising:

administering to the patient the ALK Inhibitor and an immunogenic polypeptide comprising amino acids cysteine 6 to cysteine 42 of an Epidermal Growth Factor (EGF) at an amount effective to generate an immune response against the EGF, wherein the cysteine residues are numbered relative to amino acids 1 to 52 of SEQ ID NO: 2, or an immunogenic polypeptide comprising SEQ ID NO: 2;

wherein the ALK Inhibitor is selected from the group consisting of Crizotinib, Ceritinib, Alectinib, Brigatinib, Lorlatinib, and pharmaceutically acceptable salts thereof;

wherein the ALK Inhibitor is administered in a therapeutically effective daily dose in a range of about 10 mg to about 250 mg and the immunogenic polypeptide is administered according to a therapeutically effective repeated thrice, twice or once a week, once in two weeks, once in three weeks or at least once monthly to generate polyclonal antibodies targeting EGF.

2. The method of claim 1 , wherein the immunogenic polypeptide is administered prior to the ALK Inhibitor.

3. The method of claim 1 , wherein the immunogenic polypeptide is administered at the same time as the ALK Inhibitor.

Assignments (2)
SECURITY INTEREST Recorded Feb 4, 2026
From: IN3BIO LTD.
To: WITHERS BERGMAN LLP
Reel/Frame 074607/0289 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 6, 2020
From: D'HONDT, ERIK; MOLINA-VILA, MIGUEL ANGEL
To: IN3BIO LTD.
Reel/Frame 052035/0328 →
Continuity (6)
Provisional Application 62822290 · Mar 22, 2019
Provisional Application 62760529 · Nov 13, 2018
Provisional Application 62748772 · Oct 22, 2018
Provisional Application 62727056 · Sep 5, 2018
Provisional Application 62715351 · Aug 7, 2018
Related Publication 20200046690A1 · Feb 13, 2020
References Cited (9)
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