Herceptin, developed and marketed by Roche, was the only brand of trastuzumab available in the country at the time. Initially, the court granted interim relief to the
Speaking to Daily Mirror NMRA Chairman Prof. Asita de Silva said it was a major victory for the national medicines regulator in Sri Lanka against a multi-national giant and acknowledged the support extended by the Attorney General’s Department, in particular Ms. Farzana Jameel and Ms. Chaya Sri Nammuni, for excellent legal counsel.
"Biosimilars are complex products composed of proteins, sugars or nucleic acids"
“The judgment strengthens NMRA’s resolve to increase patient access to this expensive class of medicine by registering more biosimilar medicines in Sri Lanka.”
A biosimilar medicine is described as a biological medicine that is developed, by a process of reverse engineering, to be highly-similar and clinically-equivalent to an existing biological medicine. Unlike conventional generic medicines -- which are made up of chemical compounds -- biosimilars are complex products composed of proteins, sugars or nucleic acids, or may be living entities. These products are developed to be highly-similar to an already-approved biologic medicine, known as the reference product, and have no clinically-meaningful differences in terms of safety and effectiveness from the reference product. “Biosimilar medicines provide a unique opportunity to help manage the increasing costs of biopharmaceuticals and increase patient access to this category of medicines, and competition among different biological medicines including biosimilar medicines, creates increased choice for patients and clinicians, increased commercial competition and enhanced value propositions for individual medicines” Prof. de Silva said.
"Four more brands of trastuzumab in market"
From Roche’s point of view, there is no legal framework in Sri Lanka to register biosimilar medicines. However, NMRA states that from a scientific and regulatory standpoint, the active substance of the biosimilar is just another version of the active substance of the reference product. It is widely-acknowledged that the European Medicines Agency (EMA) has the widest experience in registering biosimilars as Europe has provided market authorisation to biosimilar medicines since 2006. Therefore, NMRA is guided by EMA guidelines for registering biosimilars in Sri Lanka. According to guidelines issued by EMA, biosimilar approval/registration depends on a demonstration that chemical, physical and biological parameters are highly-similar to the reference biological product rather than a full clinical safety and efficacy programme in each indication for which the reference product is registered. “The cornerstone of any comparability exercise to establish bio-similarity is the extensive comparison of the physico-chemical and functional characteristics of the processes and molecules,” noted Dr. Kamal Jayasinghe, the Chief Executive Officer of NMRA.
NMRA further pointed out that in India, Roche litigated two biotechnology companies – Biocon and Mylan – against the manufacture and sale of their trastuzumab biosimilars in India, and at the Delhi High Court challenged the decision of the Indian drug regulator (DCGI) to register the two biosimilars for all indications of
"Roche under investigation for alleged unfair business practices"
The College of Oncologists claimed that it wasn’t an aggrieved party in this case and that trastuzumab had been used for a long time. In response to this, NMRA pointed out that it was only the Roche brand of trastuzumab (Herceptin) that was available for a long time, giving them a complete monopoly in the market. Now there are four more brands of trastuzumab available -- which is what Roche wanted to prevent. Speaking on the benefits for patients, Prof. de Silva said the price of trastuzumab 440 mg was purchased by the Health Ministry for approximately Rs.250,000 per vial when only one brand (Herceptin) was in the market. “With the registration of four trastuzumab biosimilars in Sri Lanka since 2016, NMRA has broken the monopoly enjoyed by Herceptin. Recently, the maximum tender price of trastuzumab was capped at Rs.95,000 per vial by NMRA through a gazette notification issued by the Health Minister. It is understood that an Indian-manufactured trastuzumab biosimilar -- which also holds registration with the US FDA -- has been quoted at Rs.47,000 per vial for the most recent government tender. As a result, the estimated annual saving to the government from this product alone is more than Rs.600 million. NMRA believes more patients can now be given access to this important medicine without incurring an additional burden on the National Treasury.”