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Nektar Therapeutics (NASDAQ: NKTR) reported its first-quarter 2025 financial results on May 8, 2025, revealing a significant earnings miss that sent its stock down 3.1% in after-hours trading. The quarter highlighted the challenges of transitioning from a manufacturing-focused biotech to a clinical-stage company reliant on high-stakes drug development. While the results were disappointing, the company’s pipeline advancements and upcoming clinical milestones may offer a path to recovery—if trials succeed.
Nektar’s Q1 2025 revenue plummeted 51.4% year-over-year to $10.5 million, far below analyst estimates of $15.36 million. The decline stemmed from the sale of its Huntsville manufacturing facility in December 2024, which eliminated product sales revenue. Remaining revenue came from non-cash royalty income, leaving the company with a razor-thin revenue stream.
The net loss widened to $50.9 million, or $0.24 per share, compared to a loss of $36.8 million ($0.19 per share) in Q1 2024. Excluding a $4.5 million non-cash loss from its equity method investment in Gannet BioChem, the adjusted loss was $46.4 million, still exceeding Wall Street’s expectations of a $0.16 loss per share.
Operational costs surged:
- R&D expenses rose 11.3% to $30.5 million, driven by development costs for rezpegaldesleukin (REZPEG), its lead autoimmune therapy.
- G&A expenses jumped 20.9% to $24.3 million, largely due to elevated legal costs.

Nektar’s cash reserves stood at $220.7 million as of March 31, 2025, down from $269.1 million at the end of 2024. Management projects this will be sufficient to fund operations into Q4 2026, but the company’s burn rate—$46.4 million per quarter—means it must secure positive clinical data or partnerships to extend its runway beyond 2026.
The stock’s year-to-date decline of 33.5% through May 8 starkly contrasts with the biotech sector’s 3.1% drop, underscoring investor skepticism about its ability to deliver on its pipeline.
Nektar’s future hinges on rezpegaldesleukin (REZPEG), its first-in-class T regulatory cell stimulator. Key milestones include:
- June 2025: Topline data from the Phase 2b REZOLVE-AD trial in moderate-to-severe atopic dermatitis.
- December 2025: Results from the Phase 2b REZOLVE-AA trial in alopecia areata.
- 2025: Initiation of a Phase 2 trial with TrialNet evaluating REZPEG in new-onset type 1 diabetes.
The FDA’s Fast Track designation for REZPEG in atopic dermatitis in February 2025 accelerates potential regulatory review, but success in trials is non-negotiable.
Other programs, such as NKTR-0165 (a TNFR2 antibody targeting MS and vitiligo) and NKTR-0166 (a bispecific TNFR2 antibody), are advancing into preclinical stages, with an IND submission for NKTR-0165 targeted for end-2025.
Nektar’s stock trades at a $220 million cash-equivalent valuation, excluding pipeline value. Analysts argue this undervalues the company’s potential if REZPEG’s trials succeed. However, investors must weigh this against execution risks and the $46.4 million quarterly cash burn.
The decline from $269 million to $220 million underscores the urgency of positive clinical data to attract capital.
Nektar’s Q1 2025 results reflect the growing pains of a biotech transitioning to a clinical-stage model. While the revenue miss and rising expenses are concerning, the company’s $220 million cash runway and upcoming trial readouts provide a roadmap to recovery. Investors must decide whether the risks of clinical failure and cash burn outweigh the potential rewards of a breakthrough therapy like REZPEG.
The verdict? Nektar’s stock remains a high-risk, high-reward bet. Success in its June and December 2025 trials could rekindle investor confidence and unlock value, but failure could lead to a prolonged downturn. For now, the company’s fate rests on data—no guarantees, but a clear path forward for those willing to take the gamble.
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