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Beyond Covid-19: the disruptive potential of RNA-based therapeutics

Pharmaceutical Technology

After almost seven years of research and advancement post-initial approval, ASO therapies now represent over 50% of all RNA-based therapeutics in clinical development, according to GlobalData’s pipeline product database, and may emerge as improved and highly disruptive next-generation RNA therapies.

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10 Trends and Statistics for Clinical Trials in 2023

XTalks

This article delves into ten trends and statistics in the world of clinical trials for 2023. And don’t forget to explore the upcoming webinars about clinical trials on Xtalks to see what piques your curiosity about the latest clinical trial solutions. percent, 81.1 percent, 84.9 percent and 87.2 percent.

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Roche to present a broad range of data across multiple cancer types at the ESMO Virtual Congress 2020

The Pharma Data

New and updated data from across our broad cancer portfolio including phase III results in breast, lung and prostate cancers. New integrated analyses from our tumour agnostic Rozlytrek ® (entrectinib) clinical development programme. Sign up here for the session on Saturday, 19 September, 16:00-16:30 CEST.

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CytomX Therapeutics Announces Pricing of $100 Million Public Offering of Common Stock – Jan 21, 2021

The Pharma Data

CytomX expects to use any remaining net proceeds from this offering for capital expenditures, working capital and other general corporate purposes. Copies of the preliminary prospectus supplement and the accompanying prospectus relating to these securities may also be obtained for free from: J.P.

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XELJANZ® (TOFACITINIB CITRATE) RECEIVES MARKETING AUTHORIZATION IN THE EUROPEAN UNION.

The Pharma Data

Two formulations were approved, a tablet and a new oral solution (weight-based dosing). The polyarticular JIA and juvenile PsA approval is based on data from a Phase 3 pivotal study in patients with polyarticular JIA as well as other JIA subtypes, including juvenile PsA. About the JIA Study.

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Top 30 Pharma and Biotech Companies in 2023: Statistics and Trends

XTalks

5) ProQuad/M-M-R II/Varivax ProQuad, M-M-R II and Varivax are all measles, mumps, rubella and varicella vaccines indicated for different age groups. M-M-R II was approved even earlier, in 1978. The private sector costs/dose of pediatric versions of M-M-R II, ProQuad and Varivax are $89.87, $262.37 billion in 2022.

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Pfizer and BioNTech Initiate Phase 1 Study of Single Dose mRNA-Based Combination Vaccine Candidate for Influenza and COVID-19

Pfizer

Pfizer and BioNTech Initiate Phase 1 Study of Single Dose mRNA-Based Combination Vaccine Candidate for Influenza and COVID-19. Pfizer and BioNTech Initiate Phase 1 Study of Single Dose mRNA-Based Combination Vaccine Candidate for Influenza and COVID-19. About the Phase 1 Study . Wed, 11/02/2022 - 15:44.