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Blog: Clinical trials

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Tracking the mid-year momentum of the 2026 Drugs to Watch Tracking the mid-year momentum of the 2026 Drugs to Watch
Blog July 8, 2026
Tracking the mid-year momentum of the 2026 Drugs to Watch
Biopharma Biotech Clinical trials
Bringing oncology medicines to patients faster: How Clarivate R&D Consulting supports every step to approval Bringing oncology medicines to patients faster: How Clarivate R&D Consulting supports every step to approval
Blog June 24, 2026
Bringing oncology medicines to patients faster: How Clarivate R&D Consulting supports every step to approval
ADC Biopharma Biotech
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

Clinical trials

Blog October 6, 2020
Digital innovation in drug development: Perspectives from pharma, tech and regulatory experts
Key ESMO Highlights 2020 Key ESMO Highlights 2020
Blog September 28, 2020
Key ESMO Highlights 2020
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