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Xolremdi Approved for Patients With WHIM Syndrome

The approval was based on data from the randomized, double-blind, placebo-controlled phase 3 4WHILM trial.

Teresak tarrantImmunology at duke university school of medicineDrug administrationAssociate professorDuke university school

FDA Approves Mavorixafor Capsules to Treat Patients With WHIM Syndrome

The indication is for patients aged 12 years of age and older, and the treatment is intended to increase the number of mature neutrophils and lymphocytes in patients.

Teresak tarrantPaula raganPharmaceuticals announcesDuke university school of medicineDeficiency foundationJorey berryImmune deficiency foundationSafety studyParticipants with wartsDuke university schoolFirst drug indicatedSyndrome clinicaltrials

FDA Approves Mavorixafor (XOLREMDI) as First Drug Indicated for WHIM Syndrome

FDA approves mavorixafor (XOLREMDI) for WHIM syndrome, the first approved treatment for the rate disease.

Teresak tarrantDrug administrationPharmaceuticals onImmunology at duke university school of medicinePharmaceuticals incDuke university schoolBreakthrough therapy designationNew drug application

X4 Pharmaceuticals Reports First-Quarter 2023 Financial Results and Provides Corporate Update

X4 Pharmaceuticals Reports First-Quarter 2023 Financial Results and Provides Corporate Update
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COVID-19 Collection

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