A review of SARS-CoV-2 and the ongoing clinical trials

YF Tu, CS Chien, AA Yarmishyn, YY Lin… - International journal of …, 2020 - mdpi.com
… , and molecular characteristics of SARS-CoV-2. We summarize the … of SARS-CoV-2,
which differentiate it from SARS-CoV and Middle East respiratory syndrome coronavirus (MERS-CoV

Safety, tolerability, pharmacokinetics, and immunogenicity of a monoclonal antibody (SCTA01) targeting SARS-CoV-2 in healthy adults: a randomized, double-blind …

Y Li, L Qi, H Bai, C Sun, S Xu, Y Wang… - Antimicrobial agents …, 2021 - Am Soc Microbiol
… to discontinue the dose escalation, to lower the dose, or to continue with the next dose group.
The maximum tolerated dose (MTD) was defined as the highest dose of SCTA01 at which …

Overview of approved and upcoming vaccines for SARS-CoV-2: a living review

J Alderson, V Batchelor, M O'Hanlon… - Oxford Open …, 2021 - academic.oup.com
… different strategies employed in SARS-CoV-2 vaccine development, … 1 dose-escalation
studies assessing prime and boosting at 28 days with 2, 4 and 8 µg doses, showed all doses to …

[HTML][HTML] The immunology of SARS-CoV-2 infections and vaccines

L Grigoryan, B Pulendran - Seminars in immunology, 2020 - Elsevier
… formulated mRNA vaccine encoding the trimeric SARS-CoV-2 spike protein receptor …
dose-escalation phase 1 studies of 18–55 year-old healthy adults, randomized to receive 2 doses

Immunogenicity and safety of a 3-dose regimen of a SARS-CoV-2 inactivated vaccine in adults: A randomized, double-blind, placebo-controlled phase 2 trial

J Liu, B Huang, G Li, X Chang, Y Liu… - The Journal of …, 2022 - academic.oup.com
… to receive 3 doses of 5 μg or 10 μg of a SARS-CoV-2 inactivated vaccine, or placebo separated
by 28 days. Adverse events (AEs) were recorded through day 28 after each dosing. Live …

Safety and immunogenicity of a measles-vectored SARS-CoV-2 vaccine candidate, V591/TMV-083, in healthy adults: results of a randomized, placebo-controlled …

O Launay, C Artaud, M Lachâtre, M Ait-Ahmed… - …, 2022 - thelancet.com
… We performed a randomized, placebo-controlled Phase I trial with an unblinded dose
escalation and a double-blind treatment phase at 2 sites in France and Belgium to evaluate the …

A phase I, first‐in‐human, randomized doseescalation study of anti‐activated factor XII monoclonal antibody garadacimab

A McKenzie, A Roberts, S Malandkar… - Clinical and …, 2022 - Wiley Online Library
… postulated as having a pathophysiologic role in coronavirus disease 2019 (COVID-19)
associated with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection. In …

BNT162b2 induces SARS-CoV-2-neutralising antibodies and T cells in humans

U Sahin, A Muik, I Vogler, E Derhovanessian, LM Kranz… - MedRxiv, 2020 - medrxiv.org
dosing was performed in each dose-escalation cohort. Progression in that cohort and dose
escalation … Participants received a BNT162b2 priming dose on day 1, and a booster dose on …

Safety, tolerability, pharmacokinetic characteristics, and immunogenicity of MW33: a Phase 1 clinical study of the SARS-CoV-2 RBD-targeting monoclonal antibody

X Meng, P Wang, Y Xiong, Y Wu, X Lin… - Emerging Microbes & …, 2021 - Taylor & Francis
… The current randomized, double-blind, placebo-controlled, single-dose escalation Phase
1 study investigated the safety, tolerability, immunogenicity, and PK of MW33 in healthy …

Safety and serum distribution of anti-SARS-CoV-2 monoclonal antibody MAD0004J08 after intramuscular injection

S Lanini, S Milleri, E Andreano, S Nosari… - Nature …, 2022 - nature.com
… considered a high risk also for SARS-CoV-2 infection 12,13 . … -dose, dose-escalation
study to evaluate the safety, pharmacokinetics, and virus neutralization titers of the anti-SARS-CoV-…