argenx Announces European Commission Approval of VYVGART™ (efgartigimod alfa-fcab) for the Treatment of Generalized Myasthenia Gravis
VYVGART is the first neonatal Fc receptor (FcRn) blocker approved in Europe for the treatment…
VYVGART is the first neonatal Fc receptor (FcRn) blocker approved in Europe for the treatment…
OLINVYK post-approval strategy advances with positive topline cognitive function data and continued enrollment in VOLITION…
PHILADELPHIA, Aug. 11, 2022 (GLOBE NEWSWIRE) — Cabaletta Bio, Inc. (Nasdaq: CABA), a clinical-stage biotechnology…
SOUTH SAN FRANCISCO, Calif., Aug. 11, 2022 (GLOBE NEWSWIRE) — ALX Oncology Holdings Inc., (“ALX…
Company reports second quarter XHANCE net revenue of $20.6 million increased 12% compared to second…
Presented initial data from Phase 1b trial in sickle cell disease (SCD), which demonstrate rapid…
On track to submit Investigational New Drug application to the U.S. Food and Drug Administration…
HB-200 Phase 1 data presented at ASCO met all endpoints in heavily pre-treated head and…
ANJESO® Net Product Revenue Up 49% Year-Over-Year; Vials Sold to End-Users Up 67% Year-Over-Year Dosing…
TSHA-120 treated patients in GAN demonstrated durable improvement and recoverability of sensory nerve amplitude potential…
– Enrollment of Phase 1B clinical trial of SL-172154 in combination with liposomal doxorubicin in…
— Strong cash position with $54.8 million of cash and cash equivalents as of June 30,…
MENLO PARK, Calif. and SINGAPORE, Aug. 11, 2022 (GLOBE NEWSWIRE) — ASLAN Pharmaceuticals (NASDAQ: ASLN),…
Company to Host Conference Call Today at 1:00pm ET LAVAL, Québec, Aug. 11, 2022 (GLOBE…
On track to proceed with enrollment in PRISM4 Phase 3 trial of CP101 in recurrent…
Topline data from 12-week Phase 1b trial in subjects with obesity/overweight and non-alcoholic fatty liver…
— Second quarter 2022 UPNEEQ® net product sales of $8.4 million; 42% above first quarter…
AFM13 monotherapy: On track to report topline data of the registration-directed REDIRECT trial in the…
—Sabizabulin for COVID-19 Emergency Use Authorization Application Submitted to U.S. FDA in June 2022– –The…
75% of Patients Enrolled to Date in Cohort 4 of EnACT (MAT2203 in Cryptococcal Meningitis);…