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Affibody s Licensee Rallybio Announces Preliminary Phase 1 MAD Data for RLYB116 -December 20, 2023 at 09:33 am EST

Solna, Sweden, December 20, 2023. Affibody’s licensee Rallybio Corporation today announced preliminary Phase 1 multiple ascending dose data for RLYB116, an innovative, long-acting, low volume.

David bejkerRallybio corporationPatricia industriesNordic pressLicensee rallybio announces preliminary phaseResults demonstratedMean reductionLow volume weekly subcutaneousDifferentiated therapeuticGeneralized myastheniaModular finance

Rallybio Announces Preliminary Phase 1 Multiple Ascending Dose Data for RLYB116, an Innovative Subcu

100 mg Results Demonstrated a Mean Reduction of Greater than 93% in Free C5 with Low Volume Once-a-Week Subcutaneous Dosing Data Supports the Study of RLYB116 as a Differentiated Therapeutic for the Treatment of Generalized Myasthenia Gravis Company Announces Extension of Runway to 3Q 2025 As Part of Po.

New havenUnited statesEric watskyHannah deresiewiczJorge gaetaStern investor relations incCompany announces extension of runwayProgram lead for rallybioExchange commissionRallybio corporation nasdaqTerm developmentResults demonstratedMean reductionLow volume oncea week subcutaneousDifferentiated therapeuticGeneralized myasthenia

Viking Therapeutics (VKTX) Presents New Data from Phase 2b VOYAGE Study of VK2809

Viking Therapeutics (VKTX) Presents New Data from Phase 2b VOYAGE Study of VK2809
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United statesTherapeutics incViking therapeuticsAmerican associationLiver diseasesLiver fat contentMean reductionPatients withWithout type

Intra-Cellular Therapies (ITCI) Reports Positive Topline Results from Study 403 Evaluating Lumateperone

Intra-Cellular Therapies (ITCI) Reports Positive Topline Results from Study 403 Evaluating Lumateperone
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