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Dr. Reddy’s (NYSE: RDY) debuts Obeda generic semaglutide for diabetes

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Rhea-AI Filing Summary

Dr. Reddy’s Laboratories has launched Obeda®, India’s first Drugs Controller General of India (DCGI)‑approved generic semaglutide injection for managing type 2 diabetes. The product marks a Day‑1 entry after patent expiry and targets a country with more than 101 million adults living with diabetes.

Obeda® is available in 2 mg and 4 mg pre‑filled disposable pens for once‑weekly subcutaneous use, with each pen delivering at least four weekly doses at a cost of INR 4,200 per month. A Phase III trial in 312 participants showed non‑inferior efficacy and safety versus the innovator, and Dr. Reddy’s is pairing the launch with the SemaKare™ patient‑support program and plans for broader GLP‑1 portfolios and metabolic centres of excellence in India.

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Dr. Reddy’s launches India’s first DCGI‑approved generic semaglutide, deepening its GLP‑1 diabetes franchise.

Dr. Reddy’s is entering the GLP‑1 receptor agonist space with Obeda®, India’s first DCGI‑approved generic semaglutide injection for type 2 diabetes. The product leverages in‑house API and formulation development and targets a very large domestic diabetes population.

A Phase III study in 312 participants showed Obeda® had non‑inferior efficacy and a comparable safety and immunogenicity profile to the innovator, supporting clinical credibility. The pre‑filled weekly pen format and monthly cost of INR 4,200 position the drug as a potentially accessible option in a cash‑pay market.

Strategically, management highlights GLP‑1 therapies as a focus area, with plans for a fully integrated GLP‑1 portfolio and metabolic centres of excellence, plus the SemaKare™ support program and nutrition tie‑ins. Financial impact will depend on uptake, competitive dynamics and execution in India and other phase‑1 launch countries.

 


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

 

Exhibit

Number

 

Description of Exhibits

 

 

 

99.1


Intimation dated March 21, 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

(Registrant)

 

 

Date: March 21, 2026

By:

/s/ K Randhir Singh

 

 

Name:

K Randhir Singh

 

 

Title:

Company Secretary

 

3

 

Exhibit 99.1

 


Dr. Reddy's Laboratories Ltd.

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

Hyderabad – 500 034, Telangana, India

 

CIN: L85195TG1984PLC004507

 

Tel:       + 91 40 4900 2900

Fax:     + 91 40 4900 2999

Email: mail@drreddys.com

Web:   www.drreddys.com

 

March 21, 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


Please find enclosed a Press Release viz. “Dr. Reddy’s Laboratories announces launch of India’s first DCGI-approved Semaglutide injection ‘Obeda®’ for Type 2 Diabetes.”

 

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


 



 

CONTACT

DR. REDDY'S LABORATORIES LTD.

INVESTOR RELATIONS

MEDIA RELATIONS

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

Hyderabad - 500034. Telangana, India.

AISHWARYA SITHARAM

AISHWARYASITHARAM@DRREDDYS.COM

PRIYA K

PRIYAK@DRREDDYS.COM

 

Dr. Reddy’s Laboratories announces launch of India’s first DCGI-approved
Semaglutide injection ‘Obeda®’ for Type 2 Diabetes

 

·

The announcement marks Dr. Reddy’s Day-1 entry into the GLP-1 receptor agonists therapy space and readiness to serve patients in India

·

In a head-to-head Phase-III clinical study enrolling 312 participants, Dr. Reddy’s Obeda® has shown non-inferior efficacy and similar safety to the innovator drug

·

With both API development and manufacturing, as well as formulation development conducted entirely in‐house, Obeda® underscores Dr. Reddy’s robustness in complex product development and peptide science

·

Dr. Reddy’s Obeda® semaglutide injection is available in 2 mg and 4 mg strengths and comes in a pre‐filled, disposable format for subcutaneous, once‐a-week administration with a user-friendly pen device

·

Each pen of both strengths will deliver a minimum of 4 weekly doses. The cost to the patient will be INR 4,200 per month for both strengths

·

Dr. Reddy’s aims to introduce generic semaglutide in several countries, subject to regulatory approval, as part of its phase-1 launch

·

As the company is building a full‐breadth GLP‐1 portfolio for multiple metabolic disorders, including diabetes and obesity, the brand name Obeda® was conceived to reflect this integrated therapeutic focus

 

Hyderabad, India, March 21, 2026 – Dr. Reddy’s Laboratories Ltd. (BSE: 500124, NSE: DRREDDY, NYSE: RDY, NSEIFSC: DRREDDY; along with its subsidiaries together referred to as “Dr. Reddy’s”), a global pharmaceutical company, today announced the launch of its injectable semaglutide under the brand name Obeda®, marking an important step in expanding access to advanced GLP‐1 receptor agonist–based therapy for the management of type 2 diabetes in India. Dr. Reddy’s has been the first Indian company to receive Drugs Controller General of India (DCGI) approval for generic semaglutide. This launch underscores the company’s Day‐1 entry into the segment upon patent expiry, demonstrating its readiness to serve unmet patient needs in India.

 

India faces one of the world’s largest diabetes burdens, with over 101 million adults living with the condition, according to the ICMR‐INDIAB study. The study estimates diabetes prevalence at 11.4%, with nearly four in ten adults experiencing abdominal obesity. An additional 136 million individuals are estimated to be pre‐diabetic, placing them at high risk of developing the disease. In such a scenario, semaglutide, a GLP‐1 receptor agonist, has a globally proven track record in improving glycaemic control and supporting weight management when used as part of a comprehensive treatment plan.1


 

1 https://idf.org/about-diabetes/diabetes-facts-figures/

 

 

In a head‐to‐head Phase III clinical study enrolling 312 participants, Dr. Reddy’s Obeda® established non‐inferior efficacy and a safety profile comparable to the innovator drug. It showed similar glycaemic reduction. Additionally, comparable results were observed for fasting glucose control, post‐prandial glucose control, and therapeutic glycaemic response (achieving HbA1c <7.0%) at the end of the study. No anti‐drug antibodies were detected, and the immunogenicity profile was similar to that of the innovator drug2.

 

With both API development and manufacturing, as well as formulation development conducted entirely in‐house, Obeda® reflects Dr. Reddy’s strength in complex product development and peptide science. It also showcases the company’s decade‐long expertise in peptide technology and its commitment to bringing GLP‐1 therapies to market to ensure access to high‐quality, affordable medicines and addressing India’s evolving healthcare needs. As part of its future plans for GLP-1 therapies, the company will be looking at a fully integrated API and formulation approach, encompassing both development and manufacturing in-house.

 

Erez Israeli, Chief Executive Officer of Dr. Reddy’s, said: “Today’s launch marks a significant step in our commitment to expand our portfolio in critical therapeutic areas with differentiated solutions to patients in India and across global markets. Our foray into GLP-1 therapies reflects our capabilities in complex product development and peptide science. It reinforces our vision to be a trusted partner in healthcare by combining innovation with access, ensuring advanced diabetes treatments are not only available but affordable. As part of phase-1 launch, we aim to introduce generic semaglutide in several countries and, through our ‘One Product, One Quality’ approach, we are committed to ensure the same high‐quality product across all markets.”

 

M.V. Ramana, Chief Executive Officer, Branded Markets (India and Emerging Markets), Dr. Reddy’s, said: “As the first generic semaglutide approved in the country, today’s announcement reflects our science‐led approach and our long‐standing efforts in expanding access to advanced therapies in India. With the country facing a rapidly rising diabetes burden, we aim to offer effective treatment options and enable more patients to benefit from globally established therapies. The launch of this important drug strengthens our diabetes portfolio and reinforces our broader commitment to improving long‐term health outcomes for people living with chronic metabolic diseases. GLP‐1 therapies represent an important area of focus for us, and we will continue working toward building a full‐breadth portfolio for multiple metabolic indications across all formats.”

 

Dr. Reddy’s Obeda® injection is available in 2 mg and 4 mg strengths and comes in a pre‐filled, disposable pen designed for subcutaneous, once‐a-week administration, with robust cold‐chain integrity maintained throughout distribution. Each pen of both strengths will deliver a minimum of 4 weekly doses. The cost to the patient will be INR 4,200 per month for both the strengths. Additionally, in a human‐factors study involving 41 participants completing approximately 20 key tasks aligned with the USFDA’s guidance for drug–device combination products, the Obeda® pen demonstrated non‐inferior user‐performance outcomes compared with the innovator pen3.

 

 

2 Date on file

3 Data on file

 

 

As part of its patient support programme for Obeda®, Dr. Reddy’s has developed SemaKare™, a comprehensive support system to enhance and streamline the patient journey. Supported by a digital app, SemaKare™ offers onboarding guidance, field device‐counsellor assistance, injection training, tele‐support, therapy‐adherence monitoring, and so on, to help improve treatment outcomes for patients.

 

Further, Dr. Reddy’s aims to build an integrated care ecosystem by setting up metabolic centres of excellence across India. These centres will serve as integrated hubs for advancing diabetes and other metabolic disorders treatment by focusing on healthcare professional (HCP) education, evidence-based management, and real-world evidence generation. The initiative will help in strengthening diagnostic capabilities and infrastructure, while building the skills of support staff through structured training programmes. Also, the centres will drive patient awareness and empowerment initiatives, ensuring individuals are better informed and engaged in their care journey. The centres will also feature dedicated drop box to ensure the safe and sustainable disposal of used pens. Additionally, Dr. Reddy’s aims to address the nutritional requirements of patients on GLP‐1/GIP therapies by leveraging key products from its joint venture, Dr. Reddy’s Nestlé Health Science, including Celevida GLP+, Optifast and so on. These products support improved nutrient intake and muscle mass maintenance, offering targeted nutrition that is essential for sustaining metabolic and functional health.

 

Dr. Reddy’s Obeda® is a prescription-based drug. Patients are advised to consult their doctors for more details.


 

About Dr. Reddy’s: Dr. Reddy’s Laboratories Ltd. (BSE: 500124, NSE: DRREDDY, NYSE: RDY, NSEIFSC: DRREDDY) is a global pharmaceutical company headquartered in Hyderabad, India. Established in 1984, we are committed to providing access to affordable and innovative medicines. Driven by our purpose of ‘Good Health Can’t Wait,’ we offer a portfolio of products and services including APIs, generics, branded generics, biosimilars and OTC. Our major therapeutic areas of focus are gastrointestinal, cardiovascular, diabetology, oncology, pain management and dermatology. Our major markets include – USA, India, Russia & CIS countries, China, Brazil and Europe. As a company with a history of deep science that has led to several industry firsts, we continue to plan ahead and invest in businesses of the future. As an early adopter of sustainability and ESG actions, we released our first Sustainability Report in 2004. Our current ESG goals aim to set the bar high in environmental stewardship; access and affordability for patients; diversity; and governance.

 

For more information, log on to: www.drreddys.com.


 

Disclaimer: This press release may include statements of future expectations and other forward-looking statements that are based on the management’s current views and assumptions and involve known or unknown risks and uncertainties that could cause actual results, performance or events to differ materially from those expressed or implied in such statements. In addition to statements which are forward-looking by reason of context, the words "may", "will", "should", "expects", "plans", "intends", "anticipates", "believes", "estimates", "predicts", "potential", or "continue" and similar expressions identify forward-looking statements. Actual results, performance or events may differ materially from those in such statements due to without limitation, (i) general economic conditions such as performance of financial markets, credit defaults , currency exchange rates, interest rates, persistency levels and frequency / severity of insured loss events, (ii) mortality and morbidity levels and trends, (iii) changing levels of competition and general competitive factors, (iv) changes in laws and regulations and in the policies of central banks and/or governments, (v) the impact of acquisitions or reorganization, including related integration issues, and (vi) the susceptibility of our industry and the markets addressed by our, and our customers’, products and services to economic downturns as a result of natural disasters, epidemics, pandemics or other widespread illness, including coronavirus (or COVID-19), and (vii) other risks and uncertainties identified in our public filings with the Securities and Exchange Commission, including those listed under the "Risk Factors" and "Forward-Looking Statements" sections of our Annual Report on Form 20-F for the year ended March 31, 2025. The company assumes no obligation to update any information contained herein.

 

FAQ

What did Dr. Reddy’s (RDY) announce in its latest Form 6-K?

Dr. Reddy’s announced the launch of Obeda®, India’s first DCGI‑approved generic semaglutide injection for type 2 diabetes. The product expands its GLP‑1 portfolio and targets India’s large diabetes population with a once‑weekly pre‑filled pen format and structured patient support.

What is Obeda® from Dr. Reddy’s (RDY) and how is it used?

Obeda® is Dr. Reddy’s injectable semaglutide, a GLP‑1 receptor agonist for type 2 diabetes. It comes as 2 mg and 4 mg pre‑filled, disposable pens for once‑weekly subcutaneous injections, with each pen delivering at least four weekly doses under prescription guidance from healthcare professionals.

How effective and safe is Dr. Reddy’s Obeda® semaglutide according to the filing?

In a Phase III head‑to‑head study with 312 participants, Obeda® demonstrated non‑inferior efficacy and a safety profile comparable to the innovator semaglutide. Similar glycaemic reductions, fasting and post‑prandial glucose control, HbA1c target achievement, absent anti‑drug antibodies and comparable immunogenicity were reported in the study.

What is the monthly cost of Obeda® from Dr. Reddy’s (RDY) for patients in India?

The filing states that Obeda® will cost patients INR 4,200 per month for both 2 mg and 4 mg strengths. Each pre‑filled pen provides at least four once‑weekly doses, aiming to balance advanced GLP‑1 therapy access with affordability in the Indian diabetes market.

What support programs accompany Dr. Reddy’s Obeda® launch in India?

Dr. Reddy’s is launching the SemaKare™ support program alongside Obeda®, offering onboarding guidance, device‑counsellor assistance, injection training, tele‑support and adherence monitoring. The company also plans metabolic centres of excellence and nutrition support using products like Celevida GLP+ and Optifast for GLP‑1/GIP patients.

How does Obeda® strengthen Dr. Reddy’s (RDY) long‑term GLP‑1 strategy?

Obeda® showcases Dr. Reddy’s in‑house peptide and complex product capabilities and its Day‑1 entry at patent expiry. Management outlines plans for a fully integrated GLP‑1 portfolio, covering API and formulation, multiple metabolic indications, global launches and ecosystem initiatives such as centres of excellence and digital support.

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