 "Chandrachud, CJI, D Y Chandrachud")
CJI D Y Chandrachud | (Photo: PTI)
Chief Justice of India DY Chandrachud on Saturday emphasised on the need to create awareness about rare diseases among the society, on being empathetic and supportive to such parents and their families regardless of cultural, religious or traditional barriers.
He said we can no longer afford to be unaware of genetic diseases.
Citing the National Policy of Rare Diseases launched by the Ministry of Health and Family Welfare in March 2021, he said that further research is necessary to define the definition of rare diseases and stressed on the need to ensure equitable access to advanced medical therapy like gene therapy in a diverse nation like India.
Mentioning the country’s first home-grown gene therapy for cancer which was launched by the President Droupadi Murmu in April, the CJI said, the CAR T cell therapy has often been inaccessible globally due to its prohibitive costs.
“But the therapy introduced today is not only revolutionary but also represents the world’s most affordable CAR T cell treatment, embodying the spirit of the Make in India initiative. While this innovation sparks, we face a pressing challenge ensuring access to such treatments for all patients, particularly those in underserved regions,” he said.
He also noted how people from marginalised communities face persistent barriers in accessing healthcare.
“Social determinants of health factors outside the healthcare system, such as class, caste, gender, and regional location, often play a significant role in determining an individual’s health status. Injustice in healthcare becomes evident when we view individuals not merely through the lens of clinical symptoms but by understanding their social determinants of health. This reality highlights a pressing need for targeted interventions that address these systemic barriers,” he said.
The CJI also emphasised how access to essential treatments is a fundamental aspect of the right to health, along with Article 21 of the Constitution (protection of life and personal liberty) and the need to devise strategies that enhance access to cutting edge precision diagnostics and gene therapies across the nation.
He said raising awareness among healthcare providers and patients about available treatments and ongoing clinical trials can empower more individuals to seek and receive appropriate care.
To truly address accessibility, we must confront the third key issue, which is affordability.
Recently, in a batch of petitions filed by parents of children with rare diseases, the Delhi High Court clarified that customs duties and charges should not be levied on medicines, drugs, and therapies for rare diseases, urging customs authorities to ensure these items are cleared expeditiously without unnecessary delays.
“These initiatives signify progress in our efforts to improve access to essential treatments. However, to effectively address these challenges, we must prioritise the development of indigenous technologies specifically tailored to our patient population. This involves building partnerships between research institutions, pharmaceutical companies, and the government to promote innovation in the creation of affordable therapies,” he said.
He said the government must stand behind our innovations in the treatment of rare diseases, putting its spine behind the evolution of technology.
“Support for the advancement of gene therapy and rare diseases treatment requires a multi facility approach. There are three essential types of support which are needed first for any progress to take place. The first step is society awareness. The general public must become more knowledgeable, empathetic and supportive of rare diseased patients and their families, regardless of cultural, religious or traditional barriers.
We can no longer afford to be unaware of genetic diseases,” he stressed.
Therefore, raising awareness across society about the realities of these diseases is crucial for building a culture of support, he said.
“Second, collaboration between the public and private sectors, as well as partnerships with global biotech and pharmaceutical giants has fostered a favourable environment for innovation in India….to further promote innovation in gene therapy and rare diseases, the industry must step up its support through corporate social responsibility initiatives or direct investment in startups,” Justice Chandrachud said.
He also noted that to encourage more industry participation, there should be proposals for tax incentives and benefits, especially since the market for their disease treatment is relatively small.
(Only the headline and picture of this report may have been reworked by the Business Standard staff; the rest of the content is auto-generated from a syndicated feed.)
First Published: Sep 21 2024 | 9:01 PM IST
