The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Feb. 28, 2023

Filed:

Apr. 08, 2020
Applicant:

Rottapharm Biotech S.r.l., Monza, IT;

Inventors:

Lucio Claudio Rovati, Monza, IT;

Antonio Giordani, Pavia, IT;

Filippo Magaraci, Monza, IT;

Gianfranco Caselli, Milan, IT;

Tiziana Piepoli, Milan, IT;

Daniele Maggioni, Barzio, IT;

Albino Bonazzi, Milan, IT;

Assignee:
Attorneys:
Primary Examiner:
Assistant Examiner:
Int. Cl.
CPC ...
A61K 31/438 (2006.01); A61P 35/00 (2006.01); A61K 31/4458 (2006.01); C07D 211/60 (2006.01); C07D 221/20 (2006.01); A61K 39/395 (2006.01);
U.S. Cl.
CPC ...
A61K 31/438 (2013.01); A61K 31/4458 (2013.01); A61K 39/3955 (2013.01); A61P 35/00 (2018.01); C07D 211/60 (2013.01); C07D 221/20 (2013.01);
Abstract

The present invention provides a pharmaceutical combination comprising the EP4 antagonist of Formula (R)-4-(1-(6-(4-(trifluoromethyl)benzyl)-6-azaspiro[2.5]octane-5-carboxamido)cyclopropyl)-benzoic acid or a pharmaceutically acceptable salt thereof and at least one immune checkpoint inhibitor, preferably the sodium salt of (R)-4-(1-(6-(4-(trifluoromethyl)benzyl)-6-azaspiro[2.5]octane-5-carboxamido)cyclopropyl) benzoic acid. A polymorphic form A of sodium salt of (R)-4-(1-(6-(4-(trifluoromethyl) benzyl)-6-azaspiro[2.5]octane-5-carboxamido)cyclopropyl)benzoate characterized by a powder XRD spectrum with peaks at values of the angle 2θ+0.2° of 4.3, 5.0, 5.8, 6.4, 7.1, 8.3, 8.7, 12.8, 15.3, 15.9 is also described. The combination and the polymorphic form A are described for use in the treatment of tumours.


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