IP Library Granted Patent US 11,491,152
Granted Patent B2
US 11,491,152 · App. 17/700,947 · Granted Nov 8, 2022

Methods of treating lung cancer with CYP3A4 substrate drugs

Inventors: Sundar Srinivasan (Corona Del Mar, CA); Christina Chow Wallen (Seattle, WA)
Assignee: BOW RIVER LLC
A61K31/496A61K9/0019A61K9/0053A61K9/0056A61K9/0078A61K9/0095A61K9/08A61K9/10A61K9/2004A61K9/4841A61K31/00A61K31/397A61K31/407A61K31/4468A61K31/454A61K31/4745A61K31/497A61K31/498A61K31/4995A61K31/506A61K31/519A61K31/5383A61K31/5395A61P25/16A61P25/18A61P35/02A61P35/04
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Quick Facts
Patent No.
US 11,491,152
App. No.
17/700,947
Granted
Nov 8, 2022
Kind
B2
Abstract

The present disclosure provides for methods of treating a patient with a CYP3A4 substrate drug, wherein the patient is treated with posaconazole. In some embodiments, the patient stops posaconazole treatment, waits for at least 2 days, and then is treated with the CYP3A4 substrate drug as soon as it is safe to do so. In some embodiments, treatment with the CYP3A4 substrate drug is delayed for about 2-42 days after stopping posaconazole. In some embodiments, the patient is treated with a reduced dose of the CYP3A4 substrate drug for about 2-42 days.

Claims (39)

1. A method of treating lung cancer in a patient in need thereof with an antineoplastic drug which is a CYP3A4 substrate, wherein the patient is treated with a strong CYP3A4 inhibitor, comprising:

(a) discontinuing the strong CYP3A4 inhibitor treatment;

(b) delaying administering, for at least about 4 days after discontinuing the strong CYP3A4 inhibitor treatment, a dose of the anti-neoplastic drug that the patient would have received based on the patient's age and condition if the patient had not been treated with the strong CYP3A4 inhibitor; and then

(c) administering the anti-neoplastic drug;

wherein the strong CYP3A4 inhibitor is posaconazole.

2. The method of claim 1 , wherein the patient is not obese.

3. The method of claim 1 , wherein the patient has at least one characteristic selected from the group consisting of the following:

i) body mass index (BMI) of at least about 35;

ii) waist size greater than about 42 inches;

iii) % body fat greater than about 40%;

iv) total body fat greater than about 40 kg; and,

v) medically diagnosed as obese.

4. The method of claim 1 , wherein said administering in step (c) is about 4 days to about 11 days after stopping posaconazole in step (a).

5. The method of claim 1 , wherein said administering in step (c) is about 4 days to about 9 days after stopping posaconazole in step (a).

6. The method of claim 1 , wherein said administering in step (c) is about 4 days after stopping posaconazole in step (a).

7. The method of claim 1 , wherein said administering in step (c) is about 5 days after stopping posaconazole in step (a).

8. The method of claim 1 , wherein said administering in step (c) is about 6 days after stopping posaconazole in step (a).

9. The method of claim 1 , wherein said administering in step (c) is about 7 days after stopping posaconazole in step (a).

10. The method of claim 1 , wherein said administering in step (c) is about 8 days after stopping posaconazole in step (a).

11. The method of claim 1 , wherein said administering in step (c) is about 9 days after stopping posaconazole in step (a).

12. The method of claim 1 , wherein said administering of step (c) is about 10 days after stopping posaconazole in step (a).

13. The method of claim 1 , wherein said administering in step (c) is about 11 days after stopping posaconazole in step (a).

14. The method of claim 1 , wherein said administering in step (c) is about 12 days after stopping posaconazole in step (a).

15. The method of claim 1 , wherein the lung cancer is non-small cell lung cancer (NSCLC).

16. The method of claim 1 , wherein the anti-neoplastic drug is selected from the group consisting of erlotinib, crizotinib, dabrafenib, brigatinib, lorlatinib, and trastuzumab deruxtecan.

17. The method of claim 1 , wherein the anti-neoplastic drug is erlotinib.

18. The method of claim 1 , wherein the anti-neoplastic drug is crizotinib.

19. The method of claim 1 , wherein the anti-neoplastic drug is dabrafenib.

20. The method of claim 1 , wherein the anti-neoplastic drug is brigatinib.

21. The method of claim 1 , wherein the anti-neoplastic drug is lorlatinib.

22. The method of claim 1 , wherein the anti-neoplastic drug is trastuzumab deruxtecan.

23. The method of claim 15 , wherein the NSCLC is metastatic NSCLC.

24. The method of claim 23 , wherein the metastatic NSCLC tumors are ROS1-positive.

25. The method of claim 23 , wherein the metastatic NSCLC tumors are anaplastic lymphoma kinase (ALK)-positive.

26. The method of claim 25 , wherein said administering in step (c) is about 5 days after stopping posaconazole in step (a).

27. The method of claim 25 , wherein said administering in step (c) is about 6 days after stopping posaconazole in step (a).

28. The method of claim 25 , wherein said administering in step (c) is about 7 days after stopping posaconazole in step (a).

29. The method of claim 25 , wherein said administering in step (c) is about 8 days after stopping posaconazole in step (a).

30. The method of claim 25 , wherein said administering in step (c) is about 9 days after stopping posaconazole in step (a).

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 9, 2022
From: SRINIVASAN, SUNDAR; WALLEN, CHRISTINA CHOW
To: BOW RIVER LLC
Reel/Frame 061048/0718 →
Continuity (11)
Continuation 17469628 · Sep 8, 2021
Continuation In Part 17244065 · Apr 29, 2021
Continuation 17150467 · Jan 15, 2021
Continuation 17082902 · Oct 28, 2020
Continuation 16408931 · May 10, 2019
Continuation In Part 15596585 · May 16, 2017
Continuation In Part 17407440 · Aug 20, 2021
Continuation 17099298 · Nov 16, 2020
Division 16191351 · Nov 14, 2018
Continuation In Part 15596585 · May 16, 2017
Related Publication 20220211685A1 · Jul 7, 2022
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