Skip to main content

6-K

Dr Reddys Laboratories Ltd (RDY)

6-K 2026-03-13 For: 2026-03-13
View Original
Added on April 09, 2026

SECURITIES AND EXCHANGE COMMISSION

Washington, D.C. 20549


Form 6-K

REPORT OF FOREIGN PRIVATE ISSUER PURSUANT TO RULE 13A-16 OR 15D-16

UNDER THE SECURITIES EXCHANGE ACT OF 1934


March, 2026


Commission File Number 1-15182

DR. REDDY’S LABORATORIES LIMITED

(Translation of registrant’s name into English)

8-2-337, Road No. 3, Banjara Hills

Hyderabad, Telangana 500 034, India

+91-40-49002900

(Address of principal executive office)

Indicate by check mark whether the registrant files or will file annual reports under cover of Form 20-F or Form 40-F.

Form 20-F x                                 Form 40-F ¨

Indicate by check mark if the registrant is submitting the Form 6-K in paper as permitted by Regulation S-T Rule 101(b)(1):  ______

Note:  Regulation S-T Rule 101(b)(1) only permits the submission in paper of a Form 6-K if submitted solely to provide an attached annual report to security holders.

Indicate by check mark if the registrant is submitting the Form 6-K in paper as permitted by Regulation S-T Rule 101(b)(7):  ______

Note: Regulation S-T Rule 101(b)(7) only permits the submission in paper of a Form 6-K if submitted to furnish a report or other document that the registrant foreign private issuer must furnish and make public under the laws of the jurisdiction in which the registrant is incorporated, domiciled or legally organized (the registrant’s “home country”), or under the rules of the home country exchange on which the registrant’s securities are traded, as long as the report or other document is not a press release, is not required to be and has not been distributed to the registrant’s security holders, and, if discussing a material event, has already been the subject of a Form 6-K submission or other Commission filing on EDGAR.

Indicate by check mark whether by furnishing the information contained in this Form, the registrant is also thereby furnishing the information to the Commission pursuant to Rule 12g3-2(b) under the Securities Exchange Act of 1934.

Yes  ¨                                No   x

If “Yes” is marked, indicate below the file number assigned to registrant in connection with Rule 12g3-2(b): 82-________.

EXHIBITS

ExhibitNumber Description of Exhibits
rdy0859_ex99-1.htm99.1 Intimation dated March 13, 2026
2
---

SIGNATURES

Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned, thereunto duly authorized.

DR. REDDY’S LABORATORIES LIMITED<br><br>(Registrant)
Date: March 13, 2026 By: /s/ K Randhir Singh
Name: K Randhir Singh
Title:   Company Secretary
3
---

Exhibit 99.1

Dr. Reddy's Laboratories Ltd.<br><br>8-2-337, Road No. 3, Banjara Hills<br><br>Hyderabad – 500 034, Telangana, India<br><br><br><br>CIN: L85195TG1984PLC004507<br><br>Tel:       + 91 40 4900 2900<br><br>Fax:     + 91 40 4900 2999<br><br>Email: [email protected]
Web:   www.drreddys.com

March 13, 2026

National Stock Exchange of India Ltd. (Scrip Code: DRREDDY)

BSE Limited (Scrip Code: 500124)

New York Stock Exchange Inc. (Stock Code: RDY)

NSE IFSC Ltd. (Stock Code: DRREDDY)

Dear Sir/ Madam,

Ref: Disclosure under Regulation 30 of the SEBI (Listing Obligations and Disclosure Requirements) Regulations, 2015 (“SEBI Listing Regulations”)

This is in furtherance to our intimation dated December 8, 2025, wherein we had informed that Dr. Reddy’s Laboratories SA (“Dr. Reddy’s SA”), a wholly-owned subsidiary of Dr. Reddy’s Laboratories Limited, had entered into a strategic collaboration and exclusive licensing agreement with Immutep SAS, a wholly-owned subsidiary of Immutep Limited (ASX: IMM; NASDAQ: IMMP) (“Immutep”), to develop and commercialize Eftilagimod Alfa in all countries outside North America, Europe, Japan, and Greater China.

The Company would like to inform that Immutep has announced on March 13, 2026, that the Independent Data Monitoring Committee (IDMC) for the TACTI-004 Phase III evaluating Eftilagimod alfa (“efti”) in patients in firstline non-small cell lung cancer study has recommended the discontinuation of the trial following a planned interim futility analysis, in accordance with the study protocol. This recommendation followed a review of the available safety and efficacy data.

In response to the IDMC’s recommendation, enrolment in the study will be halted and Immutep will implement an orderly wind-down of the study, including appropriate patient follow-up and site close-out in accordance with regulatory and ethical obligations. Immutep has communicated that it is undertaking a comprehensive review of the available data to better understand the results and determine the appropriate next steps for the program.

Further, Dr Reddy’s SA has, to date, made only the upfront payment to Immutep and continues to engage with Immutep on the appropriate way forward. Immutep remains focused on advancing its pipeline of innovative therapies including Eftilagimod Alpha.

This is for your information and records.

Thanking you.

Yours faithfully,

For Dr. Reddy’s Laboratories Limited

K Randhir Singh

Company Secretary, Compliance Officer & Head-CSR