PCI The Journeys Within
CPHI 2026 – 23/07/2026

Current Edition

ramusmedical
Asia Pacific

Development progress in 2018 for acute ischemic stroke drugs will fuel market growth, says GlobalData

Activase (alteplase) is currently the only FDA-approved drug available for the treatment of acute ischemic stroke (AIS) in the 8MM*; however, novel drugs designed to...
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Asia Pacific

Brand new type of cancer drug has potential to fill unmet needs in oncology market, says GlobalData

Following a study published in The Lancet Oncology regarding a brand new type of cancer drug that has shown promise in multiple cancer types in early Phase I/II tria...
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Europe

4 of the Top 7 Global CROs Have Selected Veeva Vault eTMF as Their Enterprise Standard

BARCELONA, Spain — 13 February 2019 — Veeva Systems (NYSE:VEEV) today announced four of the world’s top seven largest CROs are standardizing on V...
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Europe

SGS to Conduct its First Malaria Human Challenge Trial in Belgium

Antwerp, Belgium, February 12, 2019 SGS, a leading life-sciences, clinical and bioanalytical contract solutions provider, today announced that it will commence ...
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Asia Pacific

Despite recent setbacks, the ophthalmology market still offers vast potential, says GlobalData

Despite the ophthalmology market experiencing several research and development (R&D) setbacks during 2018, the launch of three new drugs highlights that the mark...
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news

A preliminary clinical trial shows that stem cell transplantation, along with a tolerable dose of chemotherapy, is safe and more effective at slowing down multiple sclerosis than other existing therapies.

Scientists were able to slow down MS progression in a new clinical trial using stem cell transplantation. Multiple sclerosis (MS) is a chronic neurodegener...
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news

US FDA grants Breakthrough Therapy Designation for potential next-generation RSV medicine MEDI8897

AstraZeneca and its global biologics research and development arm, MedImmune, today announced that the US Food and Drug Administration (FDA) has granted Breakthroug...
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news

FDA approves first therapy for the treatment of adult patients with a rare blood clotting disorder

The U.S. Food and Drug Administration today approved Cablivi (caplacizumab-yhdp) injection, the first therapy specifically indicated, in combination with plasma exc...
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Europe

MacroGenics breast cancer drug tops Herceptin in late-stage trial

Results from a late-stage study showed MacroGenics' experimental drug margetuximab extended progression-free survival in previously treated HER-2 positive metastatic...
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Europe

CHMP recommends approval of Praluent® (alirocumab) to reduce cardiovascular risk in people with established atherosclerotic cardiovascular disease

PARIS and TARRYTOWN, NY - February 4, 2019 - The European Medicines Agency's Committee for Medicinal Products for Human Use (CHMP) has adopted a positive opinion for...
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Quotient
CPHI 2026 – 20/07/2026