Tarpeyo Receives FDA's Green Light: A Breakthrough for IgAN Patients Facing Rapid Kidney Deterioration

LiquidityHunter · 2025-12-31T16:05:11+00:00

Calliditas Therapeutics received FDA approval for Tarpeyo, a drug targeting proteinuria in IgAN patients, triggering an 11.95% stock spike. Though it fills a treatment gap, further trials are needed to confirm its efficacy on kidney function.

LiquidityHunter

2025-12-31 16:05:11

Abstract generation in progress

Calliditas Therapeutics AB (CALT) announced a significant regulatory milestone as the U.S. Food and Drug Administration has greenlit budesonide delayed release capsules—marketed as Tarpeyo—designed to combat proteinuria in adult patients with primary IgA nephropathy (IgAN) who face accelerated disease progression. The approval applies specifically to patients with a urine protein-to-creatinine ratio (UPCR) of 1.5g/g or higher, granted through an accelerated approval pathway.

Market Response and Clinical Significance

The market responded immediately to this regulatory victory. CALT’s stock surged 11.95% during regular trading hours, closing Wednesday at $18.64, a gain of $1.99. The momentum continued in after-hours trading with an additional spike of 53.73% or $10.02 per share, reflecting investor enthusiasm for the drug’s potential commercial trajectory. The company has announced that Tarpeyo is expected to reach U.S. patients in early Q1 2022.

Understanding the Treatment Landscape

IgAN represents a rarely occurring progressive immune-mediated kidney disorder characterized by substantial clinical burden and limited treatment options. More than half of all IgAN patients face the prospect of advancing to end-stage renal disease (ESRD), underscoring the critical nature of this condition. The approval of Tarpeyo addresses a significant therapeutic gap in this patient population, offering a new avenue for proteinuria reduction.

Important Limitations and Next Steps

It is important to note that the FDA has not yet established whether Tarpeyo effectively slows the decline of kidney function in IgAN patients. Calliditas will need to conduct a confirmatory clinical trial to substantiate the drug’s clinical benefits, with continued approval contingent upon these verification results. This accelerated approval pathway reflects the agency’s commitment to addressing diseases with high unmet medical needs while gathering additional real-world evidence.

Disclaimer: These statements represent analysis and market observations, and do not constitute official FDA guidance or investment recommendations.

This page may contain third-party content, which is provided for information purposes only (not representations/warranties) and should not be considered as an endorsement of its views by Gate, nor as financial or professional advice. See Disclaimer for details.