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Uppsala, Sweden October 23, 2025. Today, Dicot Pharma announces positive topline results from its phase 2a study of LIB-01 for the treatment of erectile dysfunction. The outcomes demonstrated clinically meaningful improvements in erectile function at week 4, following a single 3-day oral treatment with LIB-01. Furthermore, the effect was sustained at week 8 and showed statistical significance in one of the pre-specified subgroups. Treatment with LIB-01 remained well tolerated. Based on the results, Dicot Pharma will now proceed with the development of LIB-01 according to plan with initiation of a phase 2b study during 2026.
Dicot Pharma’s phase 2a study (NCT06703840) aimed to investigate the efficacy and safety of the drug candidate LIB-01 for treatment of erectile dysfunction (ED). The double-blind, placebo-controlled study included 156 men, ages 26 to 65, with mild to moderate ED, classified as 11–25 on the regulatory and clinically relevant International Index of Erectile Function - Erectile Function domain score (IIEF-EF). The trial evaluated LIB-01 at three different doses, 10 mg, 25 mg, and 50 mg. Participants were assessed at four and eight weeks to evaluate the effect of LIB-01.
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NEW YORK – Swedish firm Affibody launched a new Phase II study of its HER2 PET imaging agent tezatabep matraxetan to identify metastatic breast cancer patients who may respond to treatment with Daiichi Sankyo and AstraZeneca's antibody-drug conjugate Enhertu (trastuzumab deruxtecan), the company announced Tuesday.
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A group of blind patients can now read again after being fitted with a life-changing implant at the back of the eye.
A surgeon who inserted the microchips in five patients at Moorfields Eye Hospital in London says the results of the international trial are "astounding".
Sheila Irvine, 70, who is registered blind, told the BBC it was "out of this world" to be able to read and do crosswords again. "It's beautiful, wonderful. It gives me such pleasure."
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The Nordic Life Science (NLS) Days took place this week, October 13–14, in Gothenburg, Sweden. Labiotech was on site to take the pulse of the Nordic biotech scene, and, more specifically, of Sweden’s growing role within it.
Within Sweden, Gothenburg isn’t usually the first place people think of when they picture biotech, yet a closer look reveals a city quietly becoming one of the country’s most dynamic life science hubs. You could even argue that much of what’s happening here simply doesn’t exist anywhere else.
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With a legacy rooted in global scientific excellence, Sweden is quietly building one of Europe’s most dynamic biotech ecosystems - despite lacking a big pharma anchor and facing persistent funding gaps.
- CPHI Frankfurt 2025 will highlight advancements in pharmaceutical process control, patient safety, and efficiency, addressing automation, material performance, and regulatory compliance challenges.
- BENEO's galenIQ™ excipient offers robust granule formation and high-strength tablets for continuous manufacturing, enhancing patient compliance with its pleasant taste.
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Welcome to the BioPharm International® weekly news roundup for the week of Oct. 13, 2025. In this video feature, the editors highlight each week’s industry news in an easy-to-consume, fun format. New roundups will drop every Friday, so be sure to come back each week. And be sure to check the links below for more in-depth coverage of each story.
Biologics, obesity R&D partnerships, and China collaborations are driving pharmaceutical M&A and selective venture capital funding in the third quarter of 2025, according to a new report by J.P. Morgan.
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This series, “The Situation We Faced,” is a CEO-type investigation interview into decision making, set within the context of other options, relative risk-reward situation, outcome and corporate culture ramifications, and market competitiveness positioning. So, sort of a war story reminiscence, but with clear technology or product context, some speculation about how other choices might have assisted or held things back.
As Hanns-Christian Mahler, CEO of Ten23 Health, explains the situation, “We saw up to 80% of the batch that had to be sorted out because of particulate defects in the final product, which eventually were clearly traceable to the primary packaging that was in use….
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STOCKHOLM, SWEDEN – October 9, 2025. Karolinska Development AB (Nasdaq Stockholm: KDEV) today announces that its portfolio company PharmNovo has received approval from the Spanish regulatory authorities to initiate a phase 2a clinical trial of its drug candidate, PN6047, being developed as a treatment for neuropathic pain. The trial will be conducted in the EU, but has been fully aligned with the requirements defined by the U.S. Food and Drug Administration (FDA), earlier this year.
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