Nektar Therapeutics Reports Inducement Grants Under Nasdaq Listing Rule 5635(c)(4)
Nektar Therapeutics (NASDAQ:NKTR) announced inducement grants under its 2025 Inducement Plan on February 20, 2026.
Rhea-AI Summary
Nektar Therapeutics (NASDAQ:NKTR) announced inducement grants under its 2025 Inducement Plan on February 20, 2026. The Organization and Compensation Committee granted non-qualified stock options for a total of 4,300 shares to three newly hired employees with an exercise price of $73.73 per share.
The options carry an eight-year term and vest over four years (1/4 on the one-year anniversary, then monthly 1/48th for three years), subject to continued employment and the plan and option agreement terms.
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Details
News Market Reaction – NKTR
On Mar 9, the first trading day after this news, NKTR closed 2.19% below the previous close.
Data tracked by StockTitan Argus for the Mar 9 session.
Key Figures
- Inducement options
- 4,300 shares
- Aggregate non-qualified stock options granted to three new employees
- New hires
- 3 employees
- Recipients under the 2025 Inducement Plan
- Option exercise price
- $73.73 per share
- Equal to NKTR closing price on February 20, 2026
- Option term
- 8 years
- Non-qualified stock option duration under inducement grant
- Vesting period
- 4 years
- 1/4 after one year, then monthly over next three years
- Initial vesting
- 1/4 of shares
- Cliff vesting on first anniversary of grant date
- Ongoing vesting
- 1/48 monthly
- Monthly vesting over remaining three years subject to employment
- Plan adoption date
- November 6, 2025
- Board adopted the 2025 Inducement Plan on this date
Historical Context
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Set date and time for Q4 and full-year 2025 results call.
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Announced participation in two March 2026 healthcare investor conferences.
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Collaboration with UCSF on TNFR2 antibody NKTR‑0165 in multiple sclerosis models.
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Closed underwritten equity offering raising about $460M in gross proceeds.
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Priced upsized $400M offering of shares and pre-funded warrants.
24h Move is the share-price change in the day after each event; other market factors may also have contributed.
Key Terms
non-qualified stock options financial
nasdaq listing rule 5635(c)(4) regulatory
exercise price financial
vesting financial
AI-generated analysis. How Rhea-AI works. 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 one Phase 2b clinical trial in atopic dermatitis, one Phase 2b clinical trial in alopecia areata, and 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
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