Dengue fever has been a public health crisis for decades, especially in tropical and subtropical regions, and India has been one of the worst-hit countries in recent years. With rising cases and fatal outbreaks, the country has required a reliable and inexpensive vaccine to prevent the spread of the disease. That changed with the launch of DengiAll, India's indigenous tetravalent dengue vaccine. After all these years of research, trials, and international collaboration, the vaccine is now in the last stage of testing, and a breakthrough seems at hand.

Developed by the Indian Council of Medical Research (ICMR) in collaboration with Panacea Biotech, DengiAll will be a game-changer for India's battle against dengue. The vaccine is currently in Phase 3 clinical trials, which are being conducted at 19 sites in 18 states and union territories with more than 10,335 healthy volunteers enrolled so far. The trials have shown promising results, with earlier phases (1 and 2) being successful for the vaccine to combat dengue across various strains.

The significance of the vaccine is not just its possibility in dengue prevention but also that it's an indigenous development, carefully crafted to fulfill India's needs. Balram Bhargava, former Director General of ICMR, who has played a key role in India's fight against COVID-19, ensured that India's first indigenous tetravalent dengue vaccine will be in the market by mid-2026—a landmark moment for India's health sector.

Dengue fever, transmitted by the Aedes aegypti mosquito, is one of the most common vector-borne diseases in India, especially prevalent during the monsoon season between May and September. The disease is characterized by fever, severe headache, joint pains, and sudden drop in platelet levels. It can, in severe cases, progress to dengue hemorrhagic fever (DHF) or dengue shock syndrome (DSS), which will prove fatal without urgent medical treatment. The World Health Organization (WHO) indicates that the worldwide incidence of dengue has grown eight times greater than two decades ago, thus emerging as a public health issue of major concern.

DengiAll is a tetravalent vaccine, and it has the goal of protecting against all four serotypes of the dengue virus (DENV-1, DENV-2, DENV-3, and DENV-4). This is a significant feature since dengue is a multi-serotype disease, and immunity to one serotype will not protect against others. In protecting against all four serotypes, the vaccine provides broad protection, which is extremely important in a country like India, where outbreaks are ever-present and in large part unpredictable.

The vaccine development is based on the TV003/TV005 strain, which was originally developed by the United States' National Institutes of Health (NIH). The strain was licensed to Panacea Biotech, a top Indian pharma company, and was adapted for domestic use. The company has achieved significant milestones in re-developing the vaccine to meet the specific needs of the Indian population, for whom it holds a process patent for development.

Highest Number of Cases Recorded In India

Approximately 188,401 cases were identified in 2017, with 325 deaths. Highest number of infections was reported from Tamil Nadu, followed by Kerala, Karnataka, then Punjab and West Bengal. In the 20th century, there was the significant rise in number of infections reported in 2003, 2010, 2012, and 2013, with an exponential increase beginning in 2015 onwards. During this time, repeated dengue outbreaks were reported in states of Andhra Pradesh, Goa, Delhi, Haryana, Karnataka, Gujarat, Kerala, Tamil Nadu, Punjab, and West Bengal. In 2017, dengue cases were to be the highest in India.

India, in particular, has experienced frequent outbreaks in West Bengal, Uttar Pradesh, Rajasthan, Bihar, Delhi, Kerala, and Tamil Nadu. The outbreaks have claimed thousands of lives and loaded the healthcare system with a great burden. Over 5 million cases of dengue have been reported to date as of 2023, with the Indian contribution playing a significant role in the surge. Since DengiAll is presently in its final stages of trials, the vaccine is set to reduce significantly the incidence of dengue and its complications in the country.

Why Dengue Cases Are On A Steady Rise?

Although India has been battling with dengue for years now, the illness has also been on the rise globally. The WHO states that the number of dengue cases reported globally has grown over twice in the past few years, with a total of 10.6 million cases having been reported thus far in the year 2024 alone. The growth is driven by various factors:

• Warm, humid temperatures offer ideal breeding grounds for mosquitoes.
• Overcrowded cities with poor waste management infrastructure facilitate the disease transmission.
• Increased international travel has led to dengue's expansion into non-endemic areas.

There is no cure for dengue known at the moment. It is treated with supportive care—hydration, management of fever, and close attention to platelet levels. If it is severe, hospitalization is required, and there are concerns regarding the burden this causes to the health system, especially in low-resource settings.

The presence of a dengue vaccine like DengiAll would be a welcome preventive. While a vaccine would not replace effective measures for mosquito control, it could be an extra tool in the public health arsenal, significantly reducing the number of severe cases and fatalities.

When Will Dengue Vaccine Hit the Market?

So far, DengiAll is in Phase 3 trials, and although it shows a great deal of promise, it should be kept in mind that the final approval phase could take time. If the ongoing trials continue to progress well, it is hoped that the vaccine would become available by mid-2026. This is a rough estimate, though, as it includes successful completion of the clinical trials and regulatory approvals.

Signs and Symptoms of Dengue Fever

Symptoms of dengue fever typically appear 4 to 10 days from the time of a bite from an infected mosquito and persist for 3 to 7 days. Asymptomatic cases are most common, but about 1 in 20 individuals will experience severe dengue when the initial symptoms start to resolve. Typical symptoms of dengue fever are:

• High fever
• Rash
• Severe pain behind the eyes
• Nausea and vomiting
• Muscle, bone, and joint pain

If you notice any of these symptoms, it is imperative that you receive medical care immediately, particularly if the symptoms are increasing.

How Does Vaccine Affects Dengue Treatment?

The DengiAll vaccine, India’s pioneering tetravalent dengue vaccine developed by Panacea Biotec, targets all four dengue serotypes, offering a preventive approach that could revolutionize dengue management. Dr. Divya Gopal, Consultant - Internal Medicine, Sir HN Reliance Foundation Hospital, Mumbai says, "Currently in Phase 3 trials with over 10,000 participants, it may reach markets by mid-2026 if successful. Unlike existing treatments, which focus on symptom management due to the absence of specific antivirals, DengiAll aims to reduce infection rates and disease severity, potentially lowering hospitalization and mortality, particularly during monsoon seasons. By shifting focus to prevention, DengiAll could ease the burden on healthcare systems and complement vector control efforts, significantly altering India’s dengue response strategy."

Cancer is an umbrella term for abnormal excess growth that can occur in any part of the body. Leukemia is the cancer of blood, which means there is rapid growth of abnormal blood cells. This growth starts in the bone marrow, which is where your body makes blood. The Cleveland Clinic explains that unlike other cancers, leukemia does not form a mass or tumor that can be detected in a CT scan.

The usual treatment of Leukemia involves Chemotherapy, whether by pill, injection into your vein or a shot under your skin. Another treatment for it is immunotherapy which uses a drug to boost your body’ defense system so that it can fight the cancer itself. Now, a research by American Association for Cancer Research April 2025, has revealed that a pre-made version of immunotherapy can effectively fight blood cancers. This "off-the-shelf" approach offers a potentially faster and easier way to deliver this powerful therapy to patients in need.

Promising Treatment Against Blood Cancer

This new way to treat blood cancer uses special immune cells called natural killer cells, or NK cells. These NK cells have been changed in a lab to have special tools, called CARs, that help them find and kill cancer cells. What's really helpful is that these CAR NK cells can be made ahead of time from healthy people and stored. This means doctors can just take them off the shelf and give them to patients who need them quickly, without having to wait for a treatment to be made just for them, making the whole process much simpler and faster.

The results from using this ready-made CAR NK cell treatment yielded promising results, especially for people with a type of blood cancer called acute myeloid leukemia, or AML. The scientists found that after getting this treatment, some of the patients with AML had their cancer completely disappear. This is called complete remission, and it means there were no signs of cancer left in their blood. These early successes give a lot of hope for a new and better way to treat this difficult disease.

Notably, AML is a very fast-growing and serious cancer. According to American Cancer Society this cancer develops in the myeloid cell, the cells that would normally become white blood cells. This type of cancer develops quickly, hence needs to be treated with the same urgency.

Who Does This Treatment Help?

The first group of patients who received this ready-made CAR NK cell treatment were people whose leukemia had either stopped responding to other treatments or had come back after treatment. These are often the most difficult cases to treat. The fact that some of these patients had such a good response to the SENTI-202 treatment, which is a safety feature to the SENTI-202 cells. It's like a special switch that stops the NK cells from attacking healthy cells in the body. With their cancer completely disappearing, is a very encouraging sign that this new approach could offer hope to patients who have run out of other options.

More Research Needed To Confirm Safety and Effective

The researchers are hopeful about the new treatment and early success for the treatment. They believe that this ready-made approach could lead to new types of immune therapies that are much easier to produce and give to patients. Researchers emphasized that there's a big need for better treatments for AML, and he hopes this new method can become an important option for these patients who often have very limited choices.

It's important to remember that these are just the first results from an ongoing study. The scientists are still enrolling more patients to learn even more about how safe and how well SENTI-202 works. They need to keep studying it to make sure it's a reliable and effective treatment for more people with blood cancers. Before this treatment can be used widely, the findings need to be carefully reviewed and published in a scientific journal.

The uncertainty around the Novavax's COVID-19 vaccine has been exacerbated by the Trump administration. The new government has imposed new requirements on the nation's only traditional protein-based vaccine. These new requirements have led to many confusions about vaccine updates, including other vaccines too, which await approval.

The Wait For Full Approval Is Too Long

Novavax is the maker of the protein-based COVID-19 vaccine, which was on track to receive full approval from the US Food and Drug Administration (FDA) by April 1. However, the approval process was paused because of Dr Sara Brenner, the FDA's acting commissioner. The reason for delay has raised many questions about the interference, including political, especially after Dr Peter Marks, FDA's longtime vaccine chief had left following disagreements with Health Secretary Robert F Kennedy Jr. These events have further led to the apprehensions of uncertainty regarding the vaccine's future.

As of now, Novavax's vaccine is only authorized for emergency use. Unlike mRNA vaccines form Pfizer and Moderna, which have full approval, the Novavax vaccine holds the EUA or the Emergency Use Authorization, which allows it to be distributed during public health emergencies. However, once the emergency ends, the FDA can remove these vaccines from market unless full approval is granted.

What Caused The Delay?

The FDA had initially planned to approve Novavax's vaccine by its April 1 target date. However, sources familiar with the situation revealed that Trump appointees influenced the delay. Since then, Novavax has been in discussions with the FDA to determine additional requirements for approval. In the meantime, the FDA's recent comments have fueled concerns that Novavax’s vaccine may be treated as a “new product” due to its updates to match last year’s coronavirus strain. This would require new clinical trials, a process unlikely to be completed before the fall.

ALSO READ: Novavax Says FDA Approval Back on Track for Its COVID Vaccine

This approach to Novavax’s vaccine approval stands in stark contrast to the FDA’s treatment of the mRNA vaccines, where annual strain updates have been handled in a way similar to flu vaccines, requiring only small-scale tests to demonstrate the vaccine’s continued effectiveness against new strains. Dr. Paul Offit, a vaccine expert, argued that it would be unnecessary to treat these annual updates as “new products” requiring full trials, as long as the updated vaccines show that they produce protective antibody levels.

Role Of HHS Secretary

Of course Robert F Kennedy Jr will have a role to play, being the Health Secretary, and a known vaccine skeptic. Despite claiming in recent speeches that he is not anti-vaccine, Kennedy’s past associations with anti-vaccine groups have raised alarms. His nonprofit, Children’s Health Defense, has been involved in campaigns questioning vaccine safety, and Kennedy himself has made public statements suggesting that vaccines can cause autism—a long-debunked claim.

His actions have also contributed to the uncertainty that surrounds the Novavax's approval today and the overall direction of US vaccine policies.

Is Novavax Different From Other Vaccines?

What sets Novavax apart from other COVID-19 vaccines is its traditional approach. While Pfizer and Moderna’s mRNA vaccines use genetic instructions to create a temporary version of the virus’ spike protein, Novavax’s vaccine contains lab-grown copies of the spike protein itself. This approach has been used for decades in vaccines for diseases like hepatitis B and shingles, making it a more familiar method for people who may be hesitant about mRNA vaccines.

Danish multinational pharmaceutical company Novo Nordisk has launched Wegovy in Thailand, marking the entry of its hugely popular weight loss drug in Southeast Asian market. First launched in 2021, Wegovy helped make Novo Nordisk Europe's most valuable listed company until recently, worth $615 billion at its peak. Wegovy is a semaglutide shot, which means that it is a GLP-1 receptor agonist.

"We actually received the Thai FDA approval already in 2023," said Enrico Canal Bruland, vice president and general manager of Novo's Thai subsidiary. He noted that Novo was making Wegovy available in Thailand ahead of rival Eli Lilly's Zepbound. Wegovy is currently available for prescription in private hospitals around the country and will be available soon in public hospitals. Notably, Bruland declined to provide details on Wegovy's pricing in Thailand, which has a population of around 66 million, or Novo Nordisk's plans for expansion into other Southeast Asian markets.

Notably, the most popular GLP-1 agonist Ozempic was also created by Novo Nordisk. Earlier this month, the pharma giant expanded its research in the field diabetes and weight loss drug and announced that its diabetes pill, Rybelsus, demonstrated cardiovascular benefits in a late-stage trial. The findings pave the way for the medication to become a new treatment option for people living with both diabetes and heart disease.

How Do Semaglutides Work?

Semglutide is the synthetic version of GLP-1—a natural hormone produced in the intestines that regulates blood sugar, appetite, and digestion. Now, every time you eat, your body produces various hormones, including GLP-1. These are called Post nutrition hormones, and help you absorb the energy you just consumed.

GLP-1 travels to your pancreas, prompting it to produce insulin. It also travels to the hypothalamus in your brain, which gives you the feeling of being full or satiated. Ozempic imitates this hormone, thereby, silencing the food chatter in the brain. Interestingly, for some people this food chatter is really quiet ( people with low appetite) and for others it is an outbrurst, (people who generally binge eat.) So with Ozempic, silencing this self-talk in the brain, people tend to lose their appetite and eventually weight.

However, it is important to note that losing weight includes not just fat but muscle as well. Losing too much muscle can lead to reduced strength and a shorter life span. Notably, records show that most people who start taking them stop it at 12 weeks; therefore, it is important for some but not for others.

Notably, last month, US pharma major Eli Lilly launched the obesity management drug Mounjaro in India at one-fifth of the US price. The company rolled out the drug in a single-dose vial following the marketing authorisation from the Central Drugs Standard Control Organization (CDSCO). It has been priced at Rs 3,500 for a 2.5 mg vial and Rs 4,375 for a 5 mg vial. "It is a first-of-its-kind treatment for obesity, overweight, and type 2 diabetes that activates both GIP (glucose-dependent insulinotropic polypeptide) and GLP-1 (glucagon-like peptide-1) hormone receptors," the company said.