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Blog: Clinical trials

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Europe looks to shore up global competitiveness with the E.U. Biotech Act Europe looks to shore up global competitiveness with the E.U. Biotech Act
Blog June 22, 2026
Europe looks to shore up global competitiveness with the E.U. Biotech Act
Biopharma Biotech Business Development
Using AI-powered translational safety intelligence to anticipate drug safety issues earlier Using AI-powered translational safety intelligence to anticipate drug safety issues earlier
Blog June 22, 2026
Using AI-powered translational safety intelligence to anticipate drug safety issues earlier
Biopharma Biotech Clinical trials
De-risking next-generation bispecific antibodies: a target-centric approach to safety intelligence De-risking next-generation bispecific antibodies: a target-centric approach to safety intelligence
Blog June 9, 2026
De-risking next-generation bispecific antibodies: a target-centric approach to safety intelligence
Bispecific antibodies BsAb Clinical trials
The competitive signals hiding in plain sight for biopharma The competitive signals hiding in plain sight for biopharma
Blog May 8, 2026
The competitive signals hiding in plain sight for biopharma
Biopharma Business Development Clinical trials
Why ease of administration in new drugs sometimes draws a yawn from payers Why ease of administration in new drugs sometimes draws a yawn from payers
Blog February 26, 2026
Why ease of administration in new drugs sometimes draws a yawn from payers
Biopharma Biotech Clinical trials
The path forward: What comes after a CRL? The path forward: What comes after a CRL?
Blog February 24, 2026
The path forward: What comes after a CRL?
Biopharma Biotech Clinical trials
Tolebrutinib: when safety concerns override efficacy signals Tolebrutinib: when safety concerns override efficacy signals
Blog February 24, 2026
Tolebrutinib: when safety concerns override efficacy signals
Biopharma Biotech Clinical trials
Navigating Complete Response Letters: how Clarivate solutions can help pharmas chart their path to approval Navigating Complete Response Letters: how Clarivate solutions can help pharmas chart their path to approval
Blog February 24, 2026
Navigating Complete Response Letters: how Clarivate solutions can help pharmas chart their path to approval
Biopharma Biotech Clinical trials

Clinical trials

Patient enrollment continues to be a limiting factor for trial durations Patient enrollment continues to be a limiting factor for trial durations
Blog August 10, 2020
Patient enrollment continues to be a limiting factor for trial durations
Celebrating 30 years of BioWorld Celebrating 30 years of BioWorld
Blog July 1, 2020
Celebrating 30 years of BioWorld
The trials must go on: Conducting clinical studies during the COVID-19 pandemic The trials must go on: Conducting clinical studies during the COVID-19 pandemic
Blog March 31, 2020
The trials must go on: Conducting clinical studies during the COVID-19 pandemic
COVID-19: Scientific innovation will help us beat this virus COVID-19: Scientific innovation will help us beat this virus
Blog March 25, 2020
COVID-19: Scientific innovation will help us beat this virus
Regulatory reform in China enhancing clinical trials review and approval Regulatory reform in China enhancing clinical trials review and approval
Blog August 29, 2019
Regulatory reform in China enhancing clinical trials review and approval
Blog September 1, 2018
FDA draft guidance addresses inclusion of adolescents in oncology trials
Blog February 8, 2018
FDA guidance recommends diversity in clinical trials for medical devices, but can’t require it
Blog November 30, 2017
Green light to market Hemlibra for hemophilia A with inhibitors in the US
Advances in Alzheimer’s, but Knowledge Gaps Remain Advances in Alzheimer’s, but Knowledge Gaps Remain
Blog December 14, 2016
Advances in Alzheimer’s, but Knowledge Gaps Remain