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Patient Square Makes a Big Bet on Nektar Pharmaceuticals (NKTR) Purchasing 210,000 Shares
What happened
According to a Securities and Exchange Commission (SEC) filing dated May 15, 2026, Patient Square Capital LP disclosed the purchase of 210,000 shares of Nektar Therapeutics (NKTR 4.99%). The estimated value of the trade was $11.96 million based on the average closing price for the first quarter of 2026. The quarter-end value of this new position stood at $15.11 million, reflecting the valuation shift, including price movement.
What else to know
Company overview
| Metric | Value | | --- | --- | | Price (as of market close 2026-05-15) | $70.62 | | Market Capitalization | $1.22 billion | | Revenue (TTM) | $55.63 million | | Net Income (TTM) | ($158.10 million) |
Company snapshot
Nektar Therapeutics is a clinical-stage biotechnology company focused on advancing novel immunotherapies for cancer and autoimmune conditions. Leveraging a robust pipeline and strategic collaborations with leading pharmaceutical companies, Nektar aims to address significant gaps in current treatment options. The company's expertise in cytokine engineering and immunomodulation positions it as a key innovator within the biotechnology sector.
What this transaction means for investors
If Patient Square acquired its new Nektar Therapeutics Position in the first half of the first quarter, it was a very lucrative bet for the firm. Shares of the biopharmaceutical company more than doubled in February after the company reported successful results from the phase 2b Rezolve-AD clinical trial, which treated eczema patients with rezpegaldesleukin.
Rezpegaldesleukin is an experimental treatment that targets interleukin-2 receptors. It boosts production of regulatory T cells that appear to prevent patients’ immune systems from mistakenly attacking healthy skin tissue.
The Rezolve-AD trial enrolled 393 patients. Folks randomized to receive rezpegaldesleukin once every four weeks and once every 12 weeks showed sustained disease control responses. Moreover, many patients acheived 75% and 90% skin clearance rates at the 52-week observation point, which supports quarterly dosing over time.
Nektar Therapeutics expects to advance rezpegaldesleukin into phase 3 studies soon. If all goes well, a biologic licensing application could be ready for the Food and Drug Administration to review in 2029.