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Originally anticipating an FDA decision on or before November 25, the San Carlos, Califbased company will now have to wait until 2024 due to resource constraints on behalf of the regulator, Iovance announced Thursday

With Thursdays accelerated approval, Fabhalta is now indicated for patients with IgAN who are at risk of rapid disease progression, according to Novartis, defined as patients with a urine protein-to-creatinine ratio of at least 1.5 g/g

Smeal, Cole M

Everything you need to know about lipotropic injections
