IP Library Granted Patent US 10,821,191
Granted Patent B2
US 10,821,191 · App. 15/762,171 · Granted Nov 3, 2020

SYD985 treatment of T-DM1 refractory cancer patients

Inventors: Gerrit Voortman (Nijmegen, NL); Norbert Peter Koper (Nijmegen, NL)
Assignee: Byondis B.V.
A61K47/6855A61K47/6803A61K47/6889A61P35/04C07K16/32
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 10,821,191
App. No.
15/762,171
Granted
Nov 3, 2020
Kind
B2
Abstract

The present invention relates to the duocarmycin-containing antibody-drug conjugate (ADC) trastuzumab vc-seco-DUBA (SYD985) for use in the treatment of trastuzumab emtansine (T-DM1) refractory HER2 IHC 3+ or HER2 IHC 2+/FISH positive cancer patients, particularly T-DM1 refractory breast cancer patients.

Claims (15)

1. A method of treating a trastuzumab emtansine refractory tumor, which comprises administering to a trastuzumab emtansine refractory HER2 IHC 3+ or HER2 IHC 2+/FISH positive cancer patient an effective amount of a compound of formula (I)

wherein 2.6-2.9 represent an average DAR for the compound.

2. The method according to claim 1 , wherein the average DAR for the compound is about 2.8.

3. The method according to claim 1 , wherein the patient is refractory to both trastuzumab and trastuzumab emtansine.

4. The method according to claim 1 , wherein the patient is refractory to all of trastuzumab, lapatinib and trastuzumab emtansine.

5. The method according to claim 1 , wherein the patient is a breast cancer patient.

6. The method according to claim 1 , wherein said compound is administered at a dose of from about 0.9 mg/kg to about 2.1 mg/kg of patient body weight by intravenous administration.

7. The method according to claim 6 , wherein the dose is about 0.9 mg/kg, about 1.2 mg/kg, about 1.5 mg/kg, about 1.8 mg/kg, or about 2.1 mg/kg of patient body weight.

8. The method according to claim 6 , wherein the average DAR for the compound is about 2.8.

9. The method according to claim 6 , wherein said dose is administered every 3 weeks.

10. The method according to claim 6 , wherein the patient is a breast cancer patient.

11. The method according to claim 6 , wherein said dose is about 1.2 to about 1.8 mg/kg of patient body weight.

12. The method according to claim 11 , wherein said dose is about 1.2 mg/kg of patient body weight.

13. The method according to claim 12 , wherein said dose is administered every 3 weeks.

14. The method according to claim 13 , wherein the patient is a breast cancer patient.

Assignments (2)
CHANGE OF NAME Recorded Jun 4, 2020
From: SYNTHON BIOPHARMACEUTICALS B.V.
To: BYONDIS B.V.
Reel/Frame 052844/0522 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 22, 2018
From: VOORTMAN, GERRIT; KOPER, NORBERT PETER
To: SYNTHON BIOPHARMACEUTICALS B.V.
Reel/Frame 045318/0355 →
Priority Claims (3)
EP 15186258 · Sep 22, 2015 · regional
EP 16158710 · Mar 4, 2016 · regional
EP 16169699 · May 13, 2016 · regional
Continuity (1)
Related Publication 20180280533A1 · Oct 4, 2018