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Novartis Pharmaceuticals et al. v. Dr. Reddy’s Laboratories et al. | Patent Lawsuit 1:21-cv-01106

Novartis Pharmaceuticals Corporation et al. v. Dr. Reddy’s Laboratories, Inc. et al.

1:21-cv-01106 D. Del. Closed US7973031B2
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Infringement action filed 29 Jul 2021 in the United States District Court for the District of Delaware and closed 11 Dec 2023, with US7973031B2 asserted. Recorded basis of termination: consent judgment.

Case recordPatsnap Litigation Data·

Case record

Patent involved
US7973031B2
Application no.
US10/493786
Case no.
1:21-cv-01106
Verdict cause
Infringement action
Court
D. Del.
Court level
District Court
Case region
Delaware
Chief judge
Maryellen Noreika
Trial level
First instance
Filed – Closed
29 Jul 2021 – 11 Dec 2023
Duration
865 days
Basis of termination
Consent Judgment
Products & marks
RYDAPT® Capsules, 25 mg
Validity challenges
None recorded
Source: Patsnap Litigation Data. Case 1:21-cv-01106, United States District Court for the District of Delaware. Open this record in Eureka
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Patent at issue
US7973031B2 Active App. US10/493786

Staurosporine derivatives as inhibitors of FLT3 receptor tyrosine kinase activity

The present invention relates to the use of staurosporines derivatives for the preparation of a drug for the treatment of diseases involving deregulated FLT3 receptor tyrosine kinase activity, especially for the curative and/or prophylactic treatment of leukemias and myelodysplastic syndromes, and to a method of treating diseases involving deregulated FLT3 receptor tyrosine kinase activity.

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Patent standing
Legal status
Active
Granted
5 Jul 2011
Earliest priority
30 Oct 2001
Est. expiry
9 Oct 2028
Validity challenges
None recorded
Licences recorded
None recorded
Classification
A61P35/02C07D487/04C07D519/00C07D487/14C07D498/22A61K31/535A61K31/55A61K31/155A61K31/407A61K31/553A61P19/08A61P43/00
Examiner
COLEMAN, BRENDA
Source: Patsnap patent data + case record. Bibliographic fields and drawings reproduced from the published patent document. Break down the claims
Parties & counsel

Parties of record

Counsel of record

Source: case record + Patsnap company data. Attorney names appear as recorded in the docket. Compare both portfolios
Outcome

Basis of termination

From the record · verbatim

“WHEREAS, Plaintiffs Novartis Pharmaceuticals Corporation (“Novartis”) and DanaFarber Cancer Institute, Inc. (“DFCI”), and Defendants Dr. Reddy’s Laboratories, Inc. and Dr. Reddy’s Laboratories, Ltd. (collectively, “DRL”) have agreed to terms and conditions representing a negotiated settlement of this action, have set forth those terms and conditions in a confidential Settlement and License Agreement (the “Settlement Agreement”), and have stipulated and consented to entry of this Consent Judgment and Order of Injunction; WHEREAS, for purposes of resolving this action, DRL stipulates and acknowledges that all claims of United States Patent No. 7,973,031 (the “Asserted Patent”) asserted in this action against it are valid and enforceable; and WHEREAS, for purposes of resolving this action, DRL stipulates and acknowledges that the use, sale, offer for sale, manufacture, and/or importation of the accused product (the subject of Abbreviated New Drug Application No. 215921) infringes one or more claims of the Asserted Patent asserted in this action; Case 1:21-cv-01106-MN Document 101 Filed 12/11/23 Page 1 of 4 PageID #: 4005 2 IT IS HEREBY ORDERED, DECREED, AND ADJUDGED this 11th day of December 2023: 1. Judgment is entered that the accused product (the subject of Abbreviated New Drug Application No. 215921) infringes one or more claims of the Asserted Patent asserted against DRL in this action. 2. By virtue of the license granted by Novartis to DRL as part of the Settlement Agreement, judgment is entered that there no longer exists a cause of action for infringement of the Asserted Patent by the accused product (the subject of Abbreviated New Drug Application No. 215921). 3. This Consent Judgment constitutes a “consent decree” pursuant to 21 U.S.C. § 355(j)(5)(B)(iii)(I)(bb), such that Final Approval of DRL’s Abbreviated New Drug Application No. 215921 under 21 U.S.C. § 355(j)(2)(A)(vii)(IV) may be granted on the date that this Consent Judgment is entered. 4. Pursuant to the terms of the Settlement Agreement, all other claims and counterclaims by DRL or against DRL are dismissed without prejudice. 5. This Court retains jurisdiction over all disputes arising out of the Settlement Agreement. 6. Other than as set forth in the Settlement Agreement, DRL, and its affiliates, are hereby enjoined from directly or indirectly passing title or delivering to customers in the United States the accused product (the subject of Abbreviated New Drug Application No. 215921) prior to the Generic Entry Date. 7. The injunction described in the foregoing paragraph shall take effect immediately upon entry of this Order by the Court. 8. During the term of the injunction, the Court retains jurisdiction over this action, including implementation of, or disputes arising out of, this Order of Injunction. Case 1:21-cv-01106-MN Document 101 Filed 12/11/23 Page 2 of 4 PageID #: 4006 3 9. Nothing herein prohibits or is intended to prohibit DRL from engaging in any activity permitted under 35 U.S.C. § 271(e)(1). 10. Each Party shall bear its own costs and attorney fees. 11. Each Party expressly waives any right to appeal or otherwise move for relief from this Consent Judgment and Order of Injunction.”

Case 1:21-cv-01106 · D. Del. · closed 11 December 2023
Source: case record, verbatim. The quoted paragraph is the basis-of-termination text as filed.

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Three questions this record usually leads to. Each one runs against the full litigation and patent corpus, and cites what it finds.

FAQ

Frequently asked questions

What is case 1:21-cv-01106?

1:21-cv-01106 is a patent infringement action brought by Novartis Pharmaceuticals Corporation against Dr. Reddy’s Laboratories, Inc., filed on 29 Jul 2021 in the United States District Court for the District of Delaware. The case closed on 11 December 2023.

Which patent was asserted in 1:21-cv-01106?

US7973031B2 (“Staurosporine derivatives as inhibitors of FLT3 receptor tyrosine kinase activity”), assigned to DANA-FARBER CANCER INSTITUTE INC., currently active. The record also lists RYDAPT® Capsules, 25 mg.

How was case 1:21-cv-01106 terminated?

The recorded basis of termination is consent judgment. The termination text reads: “WHEREAS, Plaintiffs Novartis Pharmaceuticals Corporation (“Novartis”) and DanaFarber Cancer Institute, Inc. (“DFCI”), and Defendants Dr. Reddy’s Laboratories, Inc. and Dr. Reddy’s Laboratories, Ltd. (collectively, “DRL”) have agreed to terms and conditions representing a negotiated settlement of this action, have set forth those terms and conditions in a confidential Settlement and License Agreement (the “Settlement Agreement”), and have stipulated and consented to entry of this Consent Judgment and Order of Injunction; WHEREAS, for purposes of resolving this action, DRL stipulates and acknow

What does dismissal without prejudice mean?

A dismissal without prejudice ends this action but leaves the claims alive — the plaintiff may file them again later, subject to the limitation period.

How long did case 1:21-cv-01106 take?

865 calendar days, from filing on 29 Jul 2021 to closure on 11 December 2023.

Who were the attorneys and the judge in 1:21-cv-01106?

Chief Judge Maryellen Noreika presided. Alexandra M. Joyce, Anne Y. Brody, Daniel M. Silver, Emil N. Nachman, Jane M. Love, Kyanna Sabanoglu, Robert W. Trenchard, Ronald A. Lee and Sung Bin Lee are recorded as counsel for plaintiff Novartis Pharmaceuticals. Anandita Vyakarnam, Beth C. Finkelstein, Constance S. Huttner, Daniel Taylor, Eve H. Ormerod, Joanna G. Goldstein and Neal C. Belgam appear for defendant Dr. Reddy’s Laboratories.

Answers reproduce fields from the case record for 1:21-cv-01106 and do not constitute legal advice. Ask your own question

Disclaimer. This page reproduces publicly available court docket data for case 1:21-cv-01106 and is provided for general information and reference only. It is not legal advice and must not be relied upon as such.

Docket data has limits. Records are drawn from a snapshot and may lag the live docket. Sealed filings, amended complaints, counterclaims and post-closure motions may not be reflected. Party names, attorney names and firm affiliations are reproduced as recorded and may contain omissions. Where a field is absent from the record, this page marks it as not recorded rather than inferring a value.

No characterisation of the parties or the outcome. This page reports what the record contains. Nothing here should be read as an assertion that any party infringed, that any patent is valid or invalid, that any settlement occurred, or that any party prevailed.

No FTO or validity opinion. Nothing on this page constitutes a freedom-to-operate, novelty, validity or infringement opinion. Any decision touching a live patent dispute should be verified independently and reviewed with qualified patent counsel.

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