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Kiora Pharmaceuticals Reports 2023 Results; Continues to Advance Pipeline of Treatments for Rare Retinal Diseases

Kiora Pharmaceuticals, Inc. today announced its 2023 financial results and provided an update on its retinal disease development pipeline. The Company s major initiatives planned for 2024 are to.

Brianm stremCalifornia newsfile corpKiora pharmaceuticals incKiora pharmaceuticalsOpen innovationMelissa toscaUpcoming milestonesOrphan drug designationsPrivate securities litigation reform actAnnual report

Kiora Pharmaceuticals, Inc : Kiora Pharmaceuticals Reports 2023 Results; Continues to Advance Pipeline of Treatments for Rare Retinal Diseases

Kiora Pharmaceuticals, Inc : Kiora Pharmaceuticals Reports 2023 Results; Continues to Advance Pipeline of Treatments for Rare Retinal Diseases
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Brianm stremDennis riedlKiora pharmaceuticals incCalifornia newsfile corpKiora pharmaceuticalsOpen innovationMelissa toscaUpcoming milestonesOrphan drug designationsPrivate securities litigation reform actAnnual report

3 Multinationals Plan Investments In Southeast Asia Facilities

3 Multinationals Plan Investments In Southeast Asia Facilities
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Taejon gwangyoksiSouth koreaInnovent biologicsKechow pharmaCompany newsBioprocessing production centerWuxi biologicsAlphamab oncologyCell reportsAustralia phaseOrphan drug designationsNeuexcell therapeutics

Immune-Onc Therapeutics Announces Orphan Drug Designation Granted by US FDA for IO-202 (Anti-LILRB4) for the Treatment of Chronic Myelomonocytic Leukemia (CMML)

Immune-Onc Therapeutics Announces Orphan Drug Designation Granted by US FDA for IO-202 (Anti-LILRB4) for the Treatment of Chronic Myelomonocytic Leukemia (CMML)
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United statesPalo altoTara cooperNational cancer instituteOnc therapeutics incGrace groupDrug administrationCalifornia institute for regenerative medicineLeukemia lymphoma society therapy acceleration programNational institutes of healthEuropean hematology associationOnc therapeuticsOrphan drug designationFast track designationFast trackOrphan drug designations

FDA Approves Iloprost Injection For the Treatment of Adults With Severe Frostbite

Iloprost had also received Priority Review and Orphan Drug Designations for this indication, and FDA approval in 2004 for the treatment of pulmonary arterial hypertension.

Norman stockbridgeActelion pharmaceuticalsPriority reviewOrphan drug designationsDrug evaluation