IP Library Granted Patent US 11,325,980
Granted Patent B2
US 11,325,980 · App. 16/085,511 · Granted May 10, 2022

Combination therapy using a LIV1-ADC and a chemotherapeutic

Inventors: Django Sussman (Seattle, WA); Fu Li (Bothell, WA); Ana Kostic (Seattle, WA)
Assignee: SEAGEN INC.
C07K16/3015A61K9/0019A61K31/337A61K31/555A61K31/704A61K39/39558A61K47/6803A61K47/6811A61K47/6851C07K16/28A61K2039/505C07K2317/24
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Quick Facts
Patent No.
US 11,325,980
App. No.
16/085,511
Granted
May 10, 2022
Kind
B2
Abstract

The invention provides methods of treating a subject having or at risk of cancer by administering a LIV-1 antibody drug conjugate and a chemotherapeutic.

Claims (12)

1. A method for treating a subject having cancer, the method comprising administering to the subject a LIV-1 antibody drug conjugate (LIV-1-ADC) and a checkpoint inhibitor, wherein the LIV-1-ADC comprises a humanized hLIV22 antibody conjugated to a vcMMAE (valine-citrulline-monomethyl auristatin E.

2. The method of claim 1 , wherein the subject has breast cancer.

3. The method of claim 2 , wherein the breast cancer is triple negative breast cancer, triple positive breast cancer, HER2-positive breast cancer, or hormone receptor positive cancer.

4. The method of claim 3 , wherein the subject has triple negative breast cancer.

5. The method of claim 1 , wherein the subject has prostate cancer, ovarian cancer, endometrial cancer, pancreatic cancer, lung cancer, a cervical cancer, a melanoma, or squamous cell carcinoma.

6. The method of claim 1 , wherein the LIV-1-ADC is administered at a dosage between 1.5 mg/kg and 4 mg/kg of the subject's body weight.

7. The method of claim 1 , wherein the LIV-1-ADC is administered at a dosage of 2.5 mg/kg of the subject's body weight.

8. The method of claim 1 , wherein the LIV-1-ADC is administered once every 3 weeks.

9. The method of claim 1 , wherein the LIV-1-ADC is administered by intravenous injection.

10. The method of claim 1 , wherein the checkpoint inhibitor is an anti-PD-1 antibody, an anti-PD-L1 antibody, an anti-CTLA4 antibody, B7-DC-Fc, LAG3, or TIM3.

11. The method of claim 10 , wherein the checkpoint inhibitor is an anti-PD-1 antibody.

12. The method of claim 11 , wherein the anti-PD-1 antibody is MEDI0680, AMP-224, nivolumab, pembrolizumab, or pidilizumab.

Assignments (1)
CHANGE OF NAME Recorded Oct 16, 2020
From: SEATTLE GENETICS, INC.
To: SEAGEN INC.
Reel/Frame 054102/0821 →
Continuity (4)
Provisional Application 62367510 · Jul 27, 2016
Provisional Application 62317792 · Apr 4, 2016
Provisional Application 62308639 · Mar 15, 2016
Related Publication 20190085091A1 · Mar 21, 2019