ANI Pharmaceuticals has secured U.S. Food and Drug Administration (FDA) approval for a new prefilled syringe format of Purified Cortrophin® Gel (repository corticotropin injection USP), marking a significant advancement in the delivery of this established therapy. The new presentation will be offered in two dosage options: 40 USP units/0.5 mL and 80 USP units/mL single-dose formats.
Enhanced Patient Experience
The prefilled syringe design represents a notable improvement in the product's administration, reducing the number of steps required for patients to receive their treatment. This development maintains the availability of the current 5 mL and 1 mL vial options while providing a more convenient alternative for patients and healthcare providers.
"Our new prefilled syringe reduces the steps required for patients to administer Cortrophin Gel treatment," stated Nikhil Lalwani, President and Chief Executive Officer of ANI. "This approval reflects our ongoing commitment to addressing the needs of those who rely on Cortrophin Gel therapy."
Therapeutic Applications
Cortrophin Gel maintains its broad range of indications for various autoimmune and inflammatory conditions. The medication is administered either subcutaneously or intramuscularly for:
- Acute episodes of rheumatic disorders including rheumatoid arthritis, juvenile rheumatoid arthritis, and psoriatic arthritis
- Management of severe acute and chronic allergic conditions affecting the eye
- Treatment of acute exacerbations of multiple sclerosis
- Symptomatic sarcoidosis
- Severe psoriasis and erythema multiforme
- Systemic lupus erythematosus and dermatomyositis
- Nephrotic syndrome without uremia
Market Availability and Strategic Impact
The new prefilled syringe format will be distributed through Cortrophin Gel's established specialty pharmacy network, with commercial launch planned for the second quarter of 2025. This development strengthens ANI Pharmaceuticals' position in the rare disease therapeutic space and demonstrates their commitment to improving treatment options for patients with complex medical conditions.
Safety Considerations
Healthcare providers should be aware of important safety considerations, including contraindications for patients with conditions such as scleroderma, osteoporosis, systemic fungal infections, and recent surgery. The medication requires careful monitoring for potential adverse reactions including infections, adrenal insufficiency, and elevated blood pressure.
The approval of this new delivery format represents a meaningful step forward in ANI Pharmaceuticals' mission of serving patients and improving lives through innovative therapeutic solutions.
