Nektar Therapeutics Reports Inducement Grants Under Nasdaq Listing Rule 5635(c)(4)
Rhea-AI Summary
Nektar Therapeutics (NASDAQ:NKTR) announced inducement grants under Nasdaq Listing Rule 5635(c)(4) for two newly hired employees totaling 18,310 non-qualified stock options under Nektar's 2025 Inducement Plan.
Grant details: 7,260 options granted on Nov 25, 2025 at an exercise price of $60.35 (closing price that day), and 11,050 options granted on Dec 4, 2025 at an exercise price of $57.69 (closing price that day). Options have an 8-year term and vest over 4 years with 1/4 vesting after one year and the remainder vesting monthly over the next three years, subject to continued employment and plan/option agreement terms.
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Key Figures
Market Reality Check
Peers on Argus
Peers show mixed moves: QURE -5.41%, PRAX +2.90%, others near flat. With NKTR down 1.03% and no broad momentum flags, trading appears stock-specific rather than a coordinated biotech sector move.
Historical Context
| Date | Event | Sentiment | Move | Catalyst |
|---|---|---|---|---|
| Nov 08 | Clinical data update | Positive | +3.6% | Phase 2b REZOLVE-AD data showed significant efficacy in asthma and dermatitis. |
| Nov 06 | Quarterly earnings | Neutral | +1.6% | Q3 2025 results with lower revenue, net loss, and cash runway into Q2 2027. |
| Oct 30 | Conference participation | Neutral | +5.3% | Announcement of Jefferies Global Healthcare Conference presentation and webcast. |
| Oct 28 | Earnings preview | Neutral | -2.6% | Scheduled date and call details for upcoming Q3 2025 financial results. |
| Oct 22 | Clinical presentation news | Positive | +4.0% | REZOLVE-AD Phase 2b data accepted for late-breaking oral presentation at ACAAI. |
Recent fundamental and clinical news (rezpegaldesleukin data, earnings, conference participation) often coincided with modest positive price reactions, suggesting the stock has recently responded constructively to clinical and corporate updates.
Over the past few months, Nektar highlighted multiple milestones. New Phase 2b REZOLVE-AD data on Nov 8, 2025 showed statistically significant efficacy and was followed by a 3.57% gain. Q3 2025 earnings on Nov 6, 2025 detailed $11.8M revenue, a $35.5M quarterly net loss, and $270.2M in cash, with a modest price uptick. Conference participation and acceptance of REZOLVE-AD data for late-breaking presentation also aligned with positive single-day moves, framing today’s inducement grants as routine alongside a backdrop of active clinical development and capital management.
Market Pulse Summary
This announcement details routine equity inducement grants totaling 18,310 non-qualified stock options to two new employees under the 2025 Inducement Plan, with market-based exercise prices and four-year vesting. It follows recent clinical progress in the REZOLVE-AD program and Q3 2025 financial disclosures. Investors may monitor future equity award activity, ongoing development milestones, and capital-raising steps as key drivers of the company’s longer-term risk and dilution profile.
Key Terms
non-qualified stock options financial
Nasdaq Listing Rule 5635(c)(4) regulatory
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).
7,260 stock options were granted to one employee on November 25, 2025 and 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