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Nektar Therapeutics Announces Research Collaboration with UCSF and Dr. Stephen Hauser for NKTR-0165, a Tumor Necrosis Factor Receptor 2 (TNFR2) Antibody, in Multiple Sclerosis

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Nektar Therapeutics (Nasdaq: NKTR) announced a research collaboration with UCSF and Dr. Stephen L. Hauser to study NKTR-0165, a first-in-class TNFR2 agonist antibody, in multiple sclerosis models. UCSF will conduct and fund the research; Nektar will supply NKTR-0165 and retain program rights.

The work will test TNFR2 agonism for neuroprotection, reduced neurodegeneration, and cell repair in neuron exposures to patient-derived B cells.

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News Market Reaction – NKTR

+3.49%
2 alerts
+3.49% Session close to close
$1.95B Market Cap
0.1x Rel. Volume

In the Feb 17 session, NKTR gained 3.49%, reflecting a moderate positive market reaction. Our momentum scanner triggered 2 alerts that day, indicating moderate trading interest and price volatility.

Data tracked by StockTitan Argus on the day of publication.

Market Context

This announcement adds an academic collaboration with UCSF and Dr. Stephen Hauser around NKTR‑0165, ...
Analysis

This announcement adds an academic collaboration with UCSF and Dr. Stephen Hauser around NKTR‑0165, a TNFR2 agonist antibody, in multiple sclerosis. It complements recent advances in Nektar’s autoimmune program rezpegaldesleukin, which showed strong Phase 2b REZOLVE‑AD data and is heading toward Phase 3. Investors may monitor how this preclinical MS work progresses, integration with Nektar’s broader pipeline strategy, and future disclosures that quantify development timelines or clinical milestones linked to NKTR‑0165.

Key Figures

Gross proceeds: $460 million Offering size: $400 million Proposed offering: $300,000,000 +5 more
8 metrics
Gross proceeds $460 million Feb 13, 2026 underwritten public offering
Offering size $400 million Upsized public offering priced Feb 11, 2026
Proposed offering $300,000,000 Proposed equity and warrant financing Feb 10, 2026
Cash & securities $229.1 million Preliminary cash and marketable securities as of Jan 31, 2026
EASI-75 maintenance 83% Patients maintaining EASI-75 at Week 52 in REZOLVE‑AD
Induction dose 24 µg/kg Q2W Agreed Phase 3 rezpegaldesleukin induction regimen
Shares offered 7,637,931 shares Common stock sold in Feb 13, 2026 offering
Shares outstanding 20,341,589 shares Common stock outstanding referenced in Schedule 13G/A

Historical Context

5 past events · Latest: Feb 13 (Negative)
Pattern 5 events
Date Event Sentiment 24h Move Catalyst
Feb 13 Offering closed Negative +0.5% Closed $460M underwritten offering of shares and pre-funded warrants.
Feb 11 Offering priced Negative +18.5% Priced upsized $400M equity offering to fund Phase 3 development.
Feb 10 Offering proposed Negative +51.1% Proposed $300M equity and warrant financing under existing shelf.
Feb 10 Phase 2b data Positive +51.1% Reported strong 36-week REZOLVE‑AD maintenance efficacy and safety data.
Feb 09 Data call notice Positive +0.7% Announced investor call to present Phase 2b REZOLVE‑AD topline results.

24h Move is the share-price change in the day after each event; other market factors may also have contributed.

Pattern Detected

Recent history shows NKTR often trading higher even around dilutive offerings, with strong upside on positive rezpegaldesleukin data.

Recent Company History

Over the last several weeks, Nektar announced positive Phase 2b REZOLVE‑AD data and plans for Phase 3, followed closely by a series of equity financings, including proposed, upsized, and completed offerings totaling several hundred million dollars in gross proceeds. Despite dilution, shares moved sharply higher on both the rezpegaldesleukin data and financing milestones, with multiple >18% to >50% daily gains. The new UCSF collaboration for NKTR‑0165 in multiple sclerosis adds an academic partnership to this backdrop of clinical progress and strengthened balance sheet.

Key Terms

tumor necrosis factor receptor 2, tnfr2, agonist antibody, regulatory t cells, +4 more
8 terms
tumor necrosis factor receptor 2 medical
"NKTR-0165 is a novel, first-in-class tumor necrosis factor receptor 2 (TNFR2) agonist antibody."
Tumor necrosis factor receptor 2 (TNFR2) is a protein on the surface of certain cells that acts like a cellular switch, detecting a messenger molecule called TNF and changing cell behavior, especially in the immune system and tissue repair. Investors care because drugs or diagnostics that target or measure TNFR2 can alter or predict disease outcomes—similar to fixing a faulty light switch to restore a room’s function—which can drive clinical success, regulatory approval, and commercial value.
tnfr2 medical
"TNFR2 signaling is an important gatekeeper of inflammation and its absence or deficit..."
TNFR2 is a protein on the surface of certain immune and other cells that acts like a lock for the signaling molecule TNF; when engaged it changes cell behavior such as promoting cell survival or regulating immune responses. Investors watch TNFR2 because drugs that block or activate it are being developed for cancer and autoimmune diseases, so clinical trial results or biomarker data tied to TNFR2 can materially affect a therapy’s commercial prospects and a company’s valuation.
agonist antibody medical
"NKTR-0165 is a novel, first-in-class tumor necrosis factor receptor 2 (TNFR2) agonist antibody."
An agonist antibody is a laboratory-made protein that binds to a specific cell surface receptor and activates it, mimicking the effect of a natural signaling molecule. For investors, these drugs matter because they can stimulate desired biological pathways (for example, boosting an immune response) and therefore represent potential therapeutic value; their ability to trigger activity rather than block it affects clinical use, development risk, and market opportunity.
regulatory t cells medical
"TNFR2 is highly expressed on regulatory T cells (Tregs), endothelial cells, and neuronal cells..."
Regulatory T cells are a specialized type of immune cell that act like a brake on the body’s defense system, preventing it from attacking healthy tissue or causing chronic inflammation. They matter to investors because drugs that increase or block these cells can change treatment success and safety in areas such as autoimmune disease, organ transplants, and cancer immunotherapy, affecting clinical trial results, approval chances, and commercial value.
tregs medical
"TNFR2 is highly expressed on regulatory T cells (Tregs), endothelial cells, and neuronal cells..."
Regulatory T cells (Tregs) are a type of immune cell that act like the body’s brakes or thermostat, keeping immune responses in balance to prevent excessive inflammation or attacks on healthy tissue. For investors, Tregs matter because therapies that increase or decrease their activity are central to treatments for autoimmune diseases, transplant rejection and some cancers; changes in clinical trial results or regulatory decisions around Treg-targeting drugs can quickly alter a company’s valuation and risk profile.
neurodegeneration medical
"explore the potential role of TNFR2 agonism in the reduction of neurodegeneration and promotion of neuroprotection..."
Neurodegeneration is the gradual damage and loss of nerve cells in the brain and nervous system, producing symptoms such as memory decline, impaired movement, or thinking problems. Think of it like electrical wiring in a house slowly fraying, which undermines how the system runs. For investors it matters because it drives demand for diagnostics, treatments and long-term care, influences regulatory risk and trial outcomes, and can significantly affect the value of health-care and biotech companies.
neuroprotection medical
"explore the potential role of TNFR2 agonism in the reduction of neurodegeneration and promotion of neuroprotection and cell repair..."
Neuroprotection are treatments or strategies aimed at preventing or slowing damage to nerve cells in the brain and nervous system, much like a helmet protects a cyclist’s head. Investors care because successful neuroprotective therapies can delay progression of chronic brain disorders, shape clinical trial design and regulatory approval paths, and create large, long-term markets for drugs or devices that preserve patients’ function and reduce healthcare costs.
b cells medical
"when neurons are exposed to patient-derived B cells. Led by Dr. Hauser..."
B cells are a type of white blood cell that act like antibody factories and memory keepers for the immune system: they produce proteins that recognize and neutralize specific pathogens and remember past infections or vaccines. Investors watch B-cell activity because many drugs and vaccines work by boosting, suppressing, or measuring these cells—so changes in B-cell data can signal a therapy’s potential effectiveness, safety profile, or market opportunity.

AI-generated analysis. How Rhea-AI works. Not financial advice.

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SAN FRANCISCO, Feb. 17, 2026 /PRNewswire/ -- Nektar Therapeutics (Nasdaq: NKTR) today announced an academic research collaboration with the University of California, San Francisco (UCSF) and Stephen L. Hauser, M.D., Robert A. Fishman Distinguished Professor of Neurology and Director of the UCSF Weill Institute for Neurosciences. Dr. Hauser is a neuroimmunologist whose research work has played a pivotal role in transforming the treatment landscape for patients with multiple sclerosis (MS).

NKTR-0165 is a novel, first-in-class tumor necrosis factor receptor 2 (TNFR2) agonist antibody. TNFR2 signaling is an important gatekeeper of inflammation and its absence or deficit is associated with a broad range of autoimmune diseases. TNFR2 is highly expressed on regulatory T cells (Tregs), endothelial cells, and neuronal cells, many of which are involved in the pathogenesis of MS.1

"We are privileged to partner with Dr. Hauser on this important research initiative to explore the role of TNFR2 agonism in several models of MS," said Jonathan Zalevsky, Ph.D., Chief Research and Development Officer of Nektar. "Dr. Hauser is a renowned and pioneering researcher in the field and his work has led to therapeutic approaches from cytokines to B-cell depleting agents that have transformed MS treatment."

The collaboration with UCSF will explore the potential role of TNFR2 agonism in the reduction of neurodegeneration and promotion of neuroprotection and cell repair when neurons are exposed to patient-derived B cells. Led by Dr. Hauser and his postdoctoral researcher Dr. Chaitrali Saha, the team at UCSF will conduct and fund all research efforts. Nektar will supply NKTR-0165 and will retain all rights to its programs under the collaboration.

"We know that TNFR2 is expressed on specific immune and CNS cells," said Dr. Hauser. "With this important research initiative, we hope to evaluate the potential neuroprotective effect associated with the agonism of this receptor for treating both MS and other neurological conditions."

In 2025, Stephen L. Hauser, M.D. won the Breakthrough Prize in Life Sciences for his work in identifying the direct cause of multiple sclerosis, which led to multiple new FDA approved therapies. As Director of the UCSF Weill Institute for Neurosciences, he leads research initiatives that link clinical and basic neurosciences at UCSF to accelerate research against neurologic diseases. His work led to the development of B cell therapies for MS patients, representing a powerful new approach for treating all forms of the disease and the first therapy of proven value for progressive MS.

About NKTR-0165 and TNFR2 Bispecific Programs

NKTR-0165 is a unique antibody agonist of the tumor necrosis factor receptor 2 (TNFR2). This investigational therapy is currently in IND-enabling studies and is being developed to address a number of autoimmune and CNS disorders, such as multiple sclerosis, vitiligo and ulcerative colitis.

Leveraging learnings from the development of NKTR-0165, the company is also developing a pipeline of TNFR2 containing bispecific molecules that pair TNFR-2 agonism with other specificities. Our lead bispecific program, known as NKTR-0166, is a unique bivalent antibody incorporating a TNFR2 agonist epitope and an antagonist epitope validated in the treatment of rheumatology diseases. As a dual agonist:antagonist of known pathways associated with key pathways linked to disease pathogenesis, this investigational antibody is being developed to address a number of rheumatic disorders.

About Multiple Sclerosis

Multiple sclerosis (MS) is a chronic, unpredictable, and often disabling disease of the central nervous system (CNS) that disrupts the flow of information within the brain and between the brain and body. It is an autoimmune disease in which the immune system's B cells attack the myelin sheath, a protective coating on nerve fibers. Affecting the brain, spinal cord and optic nerve, MS causes nerve signals to slow or stop, resulting in muscle weakness, vision loss, chronic fatigue and cognitive decline in memory, attention or processing speed. According to the National Multiple Sclerosis Society, approximately 2.9 million people globally and 1 million people in the U.S. currently have MS.2

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, California. For further information, visit www.nektar.com and follow us on LinkedIn.

Cautionary Note Regarding Forward-Looking Statements

This press release contains forward-looking statements which can be identified by words such as: "will," "develop," "potential," "evaluate," "explore," "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 United States; (vii) patents may not issue from our patent applications for our drug candidates, patents that have issued may not be enforceable, or additional intellectual property licenses from third parties may be required; and (viii) certain other important risks and uncertainties set forth in our Quarterly Report on Form 10-Q filed with the Securities and Exchange Commission on November 7, 2025. Any forward-looking statement made by us in this press release is based only on information currently available to us and speaks only as of the date on which it is made. We undertake no obligation to update any forward-looking statement, whether written or oral, that may be made from time to time, whether as a result of new information, future developments or otherwise.

University of California Disclaimer
This press release was prepared by Nektar Therapeutics and reflects solely the opinion of the company. Nothing in this statement shall be construed to imply any support or endorsement of Nektar Therapeutics, or any of its products or services, by the Regents of the University of California, its officers, agents and employees.

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

  1. Faustman DL, Davis M, Kuhtreiber WM. TNFR2 Agonism: Basic Science and Promising Treatment for Multiple Sclerosis and Related Diseases. Int J Mol Sci. 2025 Aug 14;26(16):7839. doi: 10.3390/ijms26167839. PMID: 40869160; PMCID: PMC12386426.
  2. https://www.nationalmssociety.org/

 

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SOURCE Nektar Therapeutics

FAQ

What is the Nektar (NKTR) collaboration with UCSF announced February 17, 2026?

It is an academic research collaboration to study NKTR-0165 in MS models. According to the company, UCSF and Dr. Hauser will fund and run the research while Nektar supplies NKTR-0165 and retains program rights.

What is NKTR-0165 and how does it relate to multiple sclerosis (NKTR)?

NKTR-0165 is a first-in-class TNFR2 agonist antibody being evaluated for MS. According to the company, the antibody targets TNFR2 to explore neuroprotection and reduced neurodegeneration in MS-relevant cells and models.

What will UCSF and Dr. Stephen Hauser study with NKTR-0165 for NKTR (Feb 17, 2026)?

They will evaluate TNFR2 agonism’s effect on neuroprotection, neurodegeneration reduction, and cell repair. According to the company, studies include neuron exposure to patient-derived B cells and related MS model experiments.

Who funds and conducts the research under the NKTR and UCSF collaboration announced Feb 17, 2026?

UCSF will conduct and fund all research activities, while Nektar supplies NKTR-0165 and retains program rights. According to the company, UCSF’s team led by Dr. Hauser will run the experiments and analyses.

Does the NKTR-UCSF collaboration change Nektar (NKTR) drug ownership or rights?

Nektar will retain all rights to its programs under the collaboration. According to the company, UCSF will perform and fund research but will not gain ownership of NKTR-0165 or related program rights.