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International Journal of Drug Development and Research

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Editorial - (2021) Volume 0, Issue 0

Editorial on Clinical Trials and Clinical Research on COVID 19

Shaibu Oricha *

Department of Pharmacology, University of Padova, via Ospedale Civile, Padova, Italy
*Corresponding Author:
Shaibu Oricha
Department of Pharmacology
University of Padova
via Ospedale Civile
Padova
Italy
E-mail:
Oricha@Shaibu.edu.it

Received Date: April 06, 2021; Accepted Date: April 20, 2021; Published Date: April 27, 2021

Citation: Oricha S (2021) Editorial on Clinical Trials & Clinical Research on COVID-19. Int J Drug Dev & Res Vol.13 No.S2:e002.

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Description

An article entitled “An overview of Covid-19 vaccine development worldwide” by Sachin Dwivedi deals with Covid illness 2019 (COVID-19) is an irresistible sickness brought about by a recently recognized Covid. All around the world 216 Countries and domains with 27 million COVID-19 positive cases and 0.88 million passings revealed due to Covid till 6 September, 2020. The pandemic of serious intense respiratory disorder Covid 2 (SARS-CoV-2) may be shortened by inoculation.

The innovation of an immunization is a perplexing and testing measure, which varies from the improvement of common medications. The ordinary time-frame for advancement of an immunization is 12-15 years. While the standard prescriptions are arranged towards the treatment of a problem whose side effects have emerged, immunizations are prepended for use in people not yet showing sickness indication, to forestall the event of infections.

The development and creation of a Covid antibody is a basic issue, however it is probably going to require numerous months to determine. Albeit numerous organizations have reported that the Covid immunization will be prepared soon, this will be refined to do in all actuality

Researchers started chipping away at COVID-19 antibodies during SARS flare-up, yet their endeavors didn't emerge in view of innumerous problems. Since Covid pandemic, the spread of the flare-up shows up a lot more extensive than was the situation for SARS. There is likewise the chance of the illness getting endemic and occasional in its appearance, as indicated by certain specialists. This unfurls why numerous specialists and drug offices are embraced enthusiastic endeavors to create and build up a powerful immunization against SARS-CoV-2 everywhere on the world, likewise accelerating every one of the standard stages expected to create and tryout an antibody in the human.

Another article named “Adeno-associated virus and CRISPRCas13 based system to target SARS-CoV-2 for dual therapeutic intervention” by Tanveer Ahmad gives brief about the nonpathogenic nature of adeno-related infection (AAV), they have been utilized as conveyance specialists for quality treatment. Glybera was the primary AAV (adeno related infection) based medication endorsed by European Medicines Agency (EMA) in the year 2012, trailed by FDA endorsement for Luxturna in 2017. As of now, there are in excess of 150 continuous clinical preliminaries dependent on AAV intervened quality treatment for countless illnesses including viral contaminations like HIV Depending upon their effective quality conveyance property, simplicity of union, and safe-for-human use, these little infections are presently being investigated for the restorative mediations utilizing quality altering instruments.

One such intercession can utilize focused on treatment utilizing RNA obstruction approach. Ongoing advances in CRISPR-Cas framework have prompted the disclosure of exquisite RNAsubordinate RNA-focused on nucleases, Cas13a and Cas13d, having a place with the Type VI CRISPR-Cas framework. Cas13- CRISPR-RNA complex could be an ideal apparatus to meddle with viral RNA and subsequently forestall/treat the contamination. The significant obstacle to interpret this technique lies in the capacity to convey the complex to the particular tissue contaminated by the infection. For this situation, the tainted cells are angiotensin changing over catalyst II (ACE2)- communicating type-II lung alveolar cells (SARSCoV-2 enters the cells by means of ACE2 receptor).

The groupings comparing to the variable light and hefty chain spaces could be gotten and joined by a general linker 5 to get the useful scFv. The scFv area will be in this way embedded to VP1 to acquire the VP1-scFv protein with explicit acknowledgment to ACE2 communicating cells. This methodology will be substitute to the above system. Notwithstanding, this other methodology will be relevant just for treatment reason and not for inoculation.

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