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Africa Daily Journal: Press Releases

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Press releases published on February 3, 2026

South Africans Selling Gold and Krugerrands at Record Highs
Deborah Ann Mack Fashions Celebrates Valentine’s Season With Custom Bridal and Heirloom Redesign Services
StrongMinds Partners With Zambia Correctional Service To Treat Depression Among Inmates and Officers
New E-book 'Command the Room Without Performance'
Telix Full Year Results 2025 Investor Webcast Notification
Fate Therapeutics Reports New Employee Inducement Awards Under Nasdaq Listing Rule 5635(c)(4)
Prelude Therapeutics Receives FDA Clearance of Investigational New Drug Application (IND) for PRT12396, a Mutant-selective JAK2V617F Inhibitor
Polaryx to Present Late-Breaker Data Related to SOTERIA at the 22nd Annual WORLDSymposium™ as Company Prepares for SOTERIA Trial Launch
Ardelyx Receives New Patent for Tenapanor
Beghou Names Meredith Ressi as President and Chief Growth Officer
Kyverna Therapeutics Appoints Mayo Pujols as Chief Technology Officer
Replimune Reports Fiscal Third Quarter 2026 Financial Results and Provides Corporate Update
Milestone Pharmaceuticals Reports Inducement Grants Under Nasdaq Listing Rule 5635(c)(4)
Excellent Achievements for Clearmind’s Proprietary MEAI that was Included in U.S. Congress’ Emerging Therapies Bill to Expand Veteran Access to Innovative Treatments
Highland Copper to Present at Upcoming Events
HPQ Silicon Increases Equity Stake in Novacium SAS, Strengthening Global Exposure and Short and Medium-Term Value Creation
HPQ Silicium augmente sa participation dans Novacium SAS, renforçant son exposition mondiale et la création de valeur à court et moyen terme
Invivyd Aligns with the U.S. FDA on LIBERTY, a Phase 3 Trial to Evaluate the Safety of VYD2311 Antibody Versus mRNA COVID Vaccine, and to Characterize the Safety and Immunology of Antibody and Vaccine Co-Administration
Foghorn Therapeutics to Participate in the Guggenheim Emerging Outlook: Biotech Summit
Relay Therapeutics Announces Zovegalisib Granted Breakthrough Therapy Designation by U.S. FDA for PIK3CA-mutant, HR+/HER2- Advanced Breast Cancer

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