The Union health Ministry has asked the Drugs Controller General of India to ensure equitable distribution of Remdesivir and Tocilizumab drugs, which have been included as “investigational therapies” in the national treatment protocols for Covid-19, across the country.

The aim is to ensure that their availability is not skewed and does not remain confined to metropolitan areas, an official said. The move followed after Arunachal Pradesh, Dadra and Nagar Haveli and Daman and Diu informed the ministry of the requirement of investigational therapy drugs.

Subsequently, the ministry has written to the top drug regulator, asking it to ascertain how many States and Union territories (UTs) have been covered and which of them are left, as far as the availability and distribution of these drugs by the respective companies is concerned.

“Apart from availability, the geographical distribution/reach of the drugs included as part of investigational therapies in Clinical Management Protocols for COVID-19, namely Remdesivir and Tocilizumab, may also be monitored.

“This ministry may kindly be apprised as to how many states and UTs have been covered and which of the states and UTs, if any, are left as far as the availability and distribution of these drugs by the respective companies is concerned,” the letter dated July 27 said.

The ministry has included the use of Remdesivir (for restricted emergency use purposes) and off-label application of Tocilizumab for treating Covid-19 patients in moderate stage of the illness as “investigational therapies” in the updated Clinical Management Protocol for Covid-19.

The Ministry had last year revised the prescribed dosage of anti-viral drug Remdesivir for coronavirus patients from six days to five. According to the updated version of its Clinical Management Protocol for the coronavirus , the patients must be injected with 200 milligram of Remdesivir on day one and 100 milligram for the next four days.

So far, India has reported over 15.31 lakh Covid-19 cases with over 34,000 deaths