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Wockhardt Ltd

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BSE Code : 532300 | NSE Symbol : WOCKPHARMA | ISIN : INE049B01025 | Industry : Pharmaceuticals |


Chairman's Speech

MY DEAR SHAREOWNERS

The term ‘Discovery' encapsulates the essence of Wockhardt's Research & Development (R&D) achievements and their impact on society. Like Baruch S. Blumberg, Nobel Laureate in Physiology and Medicine for his discovery of the Hepatitis B virus, said, "Discovery consists of seeing what everybody has seen and thinking what nobody has thought." ‘Life Wins' signifies the ultimate outcome of these discoveries. Every achievement in R&D brings with it the promise of alleviating suffering, extending lifespans, and bringing hope to millions of people worldwide. And I must tell you, we are now on the cusp of one of the most exciting and promising phases of Wockhardt's journey.

THE PAINSTAKING PROCESS OF DISCOVERY

Let me begin by elaborating on the incredibly long and arduous process that is involved in new drug discovery. It is a complex and multifaceted process that involves various stages, from initial research to clinical trials and regulatory approval. Like American biochemist and Nobel Laureate in Chemistry, Paul L. Modrich says, "The process of drug discovery is a testament to human ingenuity, patience, and perseverance."

The interdisciplinary expertise and knowledge resources required include a wide range of scientific disciplines, such as medicinal chemistry, microbiology, pharmacology, pharmacokinetics, animal toxicology, regulatory affairs, etc., to launch a new drug from concept to market.

The entire process begins with, sequentially, Basic Research and Target Identification, Drug Design and Development, Preclinical Studies, Investigational New Drug (IND) Application, Clinical Trials, Regulatory Review, Post-Marketing Surveillance, and Manufacturing and Distribution.

I must point out here that regulatory review is one of the most critical and complex steps involved, especially when it comes to novel antimicrobial drugs. They need huge amounts of validated data to establish their safety and efficacy as well as ensure that the New Chemical Entities (NCEs) under development are effective against existing and resistant bacterial infections.

While it takes a lot of investment, time, effort, and people at our end, we also have to collaborate, coordinate, and consult with a host of experts, professionals, companies, organisations and government departments globally before we can go to market with a new drug. They include Regulatory Agencies, Clinical Research Organisations (CROs), Academic and Research Institutions, International Health Organisations, Government Health Departments, Healthcare Providers and Hospitals, etc. At Wockhardt, we have networked and collaborated with more than 15 such organisations in our journey of new antibiotic drug discovery.

THE JOURNEY OF WOCKHARDT'S DISCOVERY PROGRAMME

As you well know, our R&D focus on discovering novel antibiotics began over 25 years ago when we recognised that new research in antibiotics was rapidly declining. Understanding the danger, and recognising the opportunity, we have consistently invested in people, processes, and technology to research our quest for novel antibiotics to face the clear and present danger, globally, of Antimicrobial Resistance (AMR).

Interestingly enough, Scottish physician and microbiologist, Sir Alexander Fleming, discoverer of Penicillin, the world's first antibiotic, was quoted thus, "The time may come when penicillin can be bought by anyone in the shops. Then there is the danger that the ignorant man may easily underdose himself and by exposing his microbes to non-lethal quantities of the drug, make them resistant." Decades later in 2016, renowned British economist Jim O'Neill, former chairman of Goldman Sachs Asset Management and erstwhile Conservative government minister, chaired a report,

‘The Review on Antimicrobial Resistance' that cited an average of 700,000 deaths attributable to AMR every year and estimated that by 2050, 10 million lives every year would be at risk due to the rise of drug-resistant infections.

Within this context, our conviction to research new antibiotics, the consistent R&D spends, and the spectacular achievements since, have vindicated and validated our dedication and focus. Today, we have six New Chemical Entities (NCEs) with Qualified Infectious Disease Product (QIDP) status from US FDA. You may be surprised to know that some of the NCEs that we are developing are being discovered after nearly 30 to 40 years in their respective classes and categories. Our first multi-spectrum anti-MRSA antibiotics launched in India, EMROK and EMROK O, have been well-received and has found traction in the medical fraternity helping successfully treat numerous patients.

We have completed Phase 3 clinical trial for WCK 4873-Nafithromycin, filed for trademark in India as MIQNAF, and are awaiting approval from the Drug Controller General of India (DCGI). We expect to launch and market it in the current financial year.

I am absolutely delighted to share with you the promising developments of our super drug WCK 5222, filed for trademark in India as ZAYNICH. Designed to address all the major Super Bugs including Pseudomonas, Klebsiella, E. coli and Acinetobacter, ZAYNICH is undergoing Global Phase 3 clinical trials which will be concluded during the financial year 2024-25. I find it very gratifying to inform you that while still under development, ZAYNICH, with due permission from the DCGI, was administered on compassionate grounds to 30 patients including 2 paediatric patients who failed to respond to any and all other antibiotics available globally. I am happy to report that it was a 100% clinical and microbiological success, saving the lives of all the recipients. Three of these cases were published in international journals across the USA (Antimicrobial Agents and Chemotherapy, American Society for Microbiology); the UK (Annals of Clinical Microbiology and Antimicrobials, Biomed Central); and the EU (European Journal of Clinical Microbiology & Infectious Diseases). Additionally, one of the cases was also presented in the prestigious Annual Conference of Clinical Infectious Disease Society, Chennai, India (CIDSCON). Further, patents for ZAYNICH have been secured in key global markets with strong IP protection, and a meropenem-resistant clinical study is set for first patient recruitment for an early launch in India. We expect global approval for ZAYNICH by the end of 2025 or in early 2026. Of course, we also continue to bolster our R&D efforts in Biologicals where we enjoy a competitive edge, especially our strong and pathbreaking presence in the diabetes segment. Our robust and focused pipeline of recombinant therapeutic proteins for insulin-resistant and higher BMI diabetic needs include recombinant Human Insulin, Insulin Glargine, and other Biosimilars like recombinant Insulin analogues (Insulin Aspart, Insulin Lispro), GLP-1 agonists, etc.

Today, our R&D investments have yielded rich returns strengthening Wockhardt's Intellectual Property (IP) base. In FY 2023-24 we filed 24 patents and were granted 30 patents, taking our cumulative patents filed to 3,263 and patents won to 840.

FUNDING WOCKHARDT'S DISCOVERY PROGRAMME

We have consistently dedicated resources towards our R&D efforts with industry-leading investments as a percentage of total revenues on a year-on-year basis. You may be interested to know that, since inception, we have invested approximately USD 500 million on our new drug discovery programme. Further, I am happy to report the successful raising of funds through the Qualified Institutional Placement route. Marquee investors like institutional giants, ICICI Prudential, Tata India Opportunities Fund, HDFC, and many other investors have participated in our offering. While a part of these funds will be used to pare our domestic debt, a significant part will be utilised to further develop our wonder drug ZAYNICH (WCK 5222) for global approval and launch. This underlines the fact that the investor community has recognised our R&D efforts, and their positive sentiment is reflected in our share performance on the bourse.

I will conclude with a quote from Jonas Salk, developer of the Polio Vaccine, who said, "The reward for work well done is the opportunity to do more." Our every success only serves to encourage us to seek and explore further. We are dedicated, committed, and focussed to do much, much, more.

Dr. Habil Khorakiwala

Founder Chairman