Nektar Therapeutics Reports Inducement Grants Under Nasdaq Listing Rule 5635(c)(4)
Rhea-AI Summary
Nektar Therapeutics (NASDAQ: NKTR) announced that on January 21, 2026 its Organization and Compensation Committee granted non-qualified stock options to purchase 1,600 shares to one newly hired employee under the 2025 Inducement Plan.
The options have an exercise price of $36.92 (closing price on January 21, 2026), an eight-year term, and vest over four years (25% after one year, then monthly 1/48ths).
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Key Figures
Market Reality Check
Peers on Argus
Before this filing, NKTR was down 1.89% while close biotech peers were mixed: SANA -2.54%, ABUS -0.24%, but PRAX, QURE, and SYRE showed gains between 1.56% and 2.71%, suggesting stock-specific rather than broad sector pressure.
Historical Context
| Date | Event | Sentiment | Move | Catalyst |
|---|---|---|---|---|
| Dec 16 | Phase 2b results | Positive | -7.8% | REZOLVE-AA Phase 2b topline showed strong signals but missed primary endpoint. |
| Dec 15 | Conference call notice | Neutral | -2.6% | Announcement of investor call to review upcoming REZOLVE-AA topline data. |
| Dec 05 | Inducement grants | Neutral | +0.7% | Disclosure of 18,310 inducement stock options to two new employees. |
| Nov 08 | Clinical data update | Positive | +3.6% | REZOLVE-AD Phase 2b data showed significant asthma and dermatitis improvements. |
| Nov 06 | Earnings report | Neutral | +1.6% | Q3 2025 results with $270.2M cash and revenue decline after facility sale. |
Recent major clinical and earnings updates generally aligned with price moves, while one mixed but largely positive alopecia readout saw a sharp negative reaction.
Over the last few months, Nektar reported several key updates. A Dec 16, 2025 REZOLVE-AA Phase 2b topline readout showed efficacy signals but missed the primary endpoint in the main analysis, and shares fell 7.77%. Earlier, REZOLVE-AD Phase 2b data on Nov 8, 2025 showed statistically significant improvements and the stock rose 3.57%. Q3 2025 earnings on Nov 6, 2025 highlighted $270.2M in cash and support into Q2 2027, with a 1.58% gain. A prior inducement grant disclosure on Dec 5, 2025 saw a modest 0.67% uptick.
Market Pulse Summary
This announcement details a standard inducement grant of 1,600 non-qualified stock options under Nektar’s 2025 Inducement Plan, with an exercise price of $36.92, an eight-year term, and four-year vesting. It follows a period of active clinical and regulatory news flow, including recent REZOLVE-AA and REZOLVE-AD updates and Q3 2025 financials. Investors may watch upcoming February 2026 communications and further trial milestones for more consequential catalysts than this administrative equity action.
Key Terms
nasdaq listing rule 5635(c)(4) regulatory
non-qualified stock options financial
exercise price financial
AI-generated analysis. Not financial advice.
Nektar's 2025 Inducement Plan was adopted by its Board of Directors on November 6, 2025 and is used exclusively for the grant of equity awards to individuals who were not previously an employee or non-employee director of Nektar (or following a bona fide period of non-employment), as an inducement material to such individual's entering into employment with Nektar, pursuant to Nasdaq Listing Rule 5635(c)(4).
The stock options have an exercise price per share equal to
About Nektar Therapeutics
Nektar Therapeutics is a clinical-stage biotechnology company focused on developing treatments that address the underlying immunological dysfunction in autoimmune and chronic inflammatory diseases. Nektar's lead product candidate, rezpegaldesleukin (REZPEG, or NKTR-358), is a novel, first-in-class regulatory T cell stimulator being evaluated in two Phase 2b clinical trials, one in atopic dermatitis, one in alopecia areata, and in one Phase 2 clinical trial in Type 1 diabetes mellitus. Nektar's pipeline also includes a preclinical bivalent tumor necrosis factor receptor type II (TNFR2) antibody and bispecific programs, NKTR-0165 and NKTR-0166, and a modified hematopoietic colony stimulating factor (CSF) protein, NKTR-422. Nektar, together with various partners, is also evaluating NKTR-255, an investigational IL-15 receptor agonist designed to boost the immune system's natural ability to fight cancer, in several ongoing clinical trials.
Nektar is headquartered in San Francisco,
Cautionary Note Regarding Forward-Looking Statements
This press release contains forward-looking statements which can be identified by words such as: "could," "develop," "evaluate," "address," "may" and similar references to future periods. Examples of forward-looking statements include, among others, statements regarding the therapeutic potential of, and future development plans for, rezpegaldesleukin, NKTR-0165, NKTR-0166, NKTR-422, and NKTR-255. Forward-looking statements are neither historical facts nor assurances of future performance. Instead, they are based only on our current beliefs, expectations and assumptions regarding the future of our business, future plans and strategies, anticipated events and trends, the economy and other future conditions. Because forward-looking statements relate to the future, they are subject to inherent uncertainties, risks and changes in circumstances that are difficult to predict and many of which are outside of our control. Our actual results may differ materially from those indicated in the forward-looking statements. Therefore, you should not rely on any of these forward-looking statements. Important factors that could cause our actual results to differ materially from those indicated in the forward-looking statements include, among others: (i) our statements regarding the therapeutic potential of rezpegaldesleukin, NKTR-0165, NKTR-0166, NKTR-422 and NKTR-255 are based on preclinical and clinical findings and observations and are subject to change as research and development continue; (ii) rezpegaldesleukin, NKTR-0165, NKTR-0166, NKTR-422 and NKTR-255 are investigational agents and continued research and development for these drug candidates is subject to substantial risks, including negative safety and efficacy findings in future clinical studies (notwithstanding positive findings in earlier preclinical and clinical studies); (iii) rezpegaldesleukin, NKTR-0165, NKTR-0166, NKTR-422 and NKTR-255 are in clinical development and the risk of failure is high and can unexpectedly occur at any stage prior to regulatory approval; (iv) data reported from ongoing clinical trials are necessarily interim data only and the final results will change based on continuing observations; (v) the timing of the commencement or end of clinical trials and the availability of clinical data may be delayed or unsuccessful due to regulatory delays, slower than anticipated patient enrollment, manufacturing challenges, changing standards of care, evolving regulatory requirements, clinical trial design, clinical outcomes, competitive factors, or delay or failure in ultimately obtaining regulatory approval in one or more important markets; (vi) a Fast Track designation does not increase the likelihood that rezpegaldesleukin will receive marketing approval in the
Contacts:
For Investors:
Vivian Wu
VWu@nektar.com
Corey Davis, Ph.D.
LifeSci Advisors, LLC
cdavis@lifesciadvisors.com
212-915-2577
Ahu Demir, Ph.D.
LifeSci Advisors, LLC
ademir@lifesciadvisors.com
212-915-3820
For Media:
Jonathan Pappas
LifeSci Communications
857-205-4403
jpappas@lifescicomms.com
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SOURCE Nektar Therapeutics