Welcome to our dedicated page for Nektar Therapeutics news (Ticker: NKTR), a resource for investors and traders seeking the latest updates and insights on Nektar Therapeutics stock.
Nektar Therapeutics (Nasdaq: NKTR) generates a steady flow of news tied to its role as a clinical-stage biotechnology company focused on autoimmune and chronic inflammatory diseases. Company announcements emphasize progress with its lead product candidate, rezpegaldesleukin (REZPEG, or NKTR-358), a regulatory T cell stimulator and IL-2 pathway agonist being evaluated in multiple mid-stage trials.
News coverage frequently highlights clinical data from the REZOLVE-AD Phase 2b study in moderate-to-severe atopic dermatitis and the REZOLVE-AA Phase 2b study in severe-to-very-severe alopecia areata. Press releases describe topline results, detailed efficacy and safety outcomes, and analyses in subgroups such as patients with atopic dermatitis and a history of asthma, including Asthma Control Questionnaire (ACQ-5) findings.
Investors and observers can also find updates on regulatory interactions, such as the U.S. Food and Drug Administration granting Fast Track designations for rezpegaldesleukin in atopic dermatitis and alopecia areata. Additional news items cover Nektar’s participation in scientific and investor conferences, late-breaking oral presentations at major dermatology and allergy meetings, and corporate events like equity offerings and compliance updates related to its Nasdaq Capital Market listing.
This news page aggregates these disclosures so readers can follow developments in Nektar’s immunology pipeline, including rezpegaldesleukin and other programs such as NKTR-0165, NKTR-0166, NKTR-422 and NKTR-255. For those tracking NKTR stock or the evolution of Treg-focused therapies, this feed provides a centralized view of clinical milestones, financial communications and key corporate announcements.
Nektar Therapeutics (NASDAQ:NKTR) announced the dosing of the first patient in a Phase 1/2 trial of NKTR-255, aimed at treating relapsed/refractory head and neck squamous cell carcinoma and colorectal cancer. The trial involves up to 80 patients across 15 sites in the U.S. and EU, assessing NKTR-255 alongside cetuximab. NKTR-255 activates the IL-15 pathway, promoting NK and CD8+ T cell expansion without suppressive regulatory T cells. Initial data showed NKTR-255 was well tolerated and biologically active, enhancing lymphocyte expansion.
Nektar Therapeutics (NASDAQ: NKTR) presented nonclinical data for its IL-15 pathway agonist, NKTR-255, at the 62nd ASH Annual Meeting. The research, in collaboration with Dana-Farber Cancer Center, highlights NKTR-255's potential to enhance natural killer (NK) cell and memory CD8 T cell functions. Currently in Phase 1b/2 studies, NKTR-255 aims to combine with agents like rituximab for treating multiple myeloma (MM) and non-Hodgkin's lymphoma (NHL), showing promising anti-tumor activity.
Nektar Therapeutics (NKTR) announced notable data presentations regarding its immuno-oncology pipeline at the 2020 Society for Immunotherapy of Cancer Annual Meeting. Key developments include the PIVOT-02 study data for BEMPEG plus nivolumab, showing a 53% overall response rate and a 30.9-month median progression-free survival in Stage IV melanoma patients. NKTR also reported promising results for NKTR-262 and NKTR-255, with biological activity demonstrated in patients with hematologic malignancies. The findings underscore the potential of Nektar's therapies to effectively enhance anti-cancer immunity.
Nektar Therapeutics (NASDAQ:NKTR) announced a webcast conference call on November 11, 2020, at 4:15 p.m. EST featuring oncology experts and company management. The event coincides with the 2020 Society for Immunotherapy of Cancer Annual Meeting. Key topics include clinical data from three studies, notably the PIVOT-02 study involving bempegaldesleukin (NKTR-214) and nivolumab. Notable presenters include Drs. Adi Diab, Brendan Curti, and Nina Shah. Interested parties can access the call via dial-in or live audio webcast, with a replay available for two weeks.
Nektar Therapeutics (NKTR) reported Q3 2020 financial results showing revenue growth to $30.0 million from $29.2 million in Q3 2019, and a year-to-date revenue of $129.5 million, up from $80.8 million in the same period last year, driven by milestone payments from Bristol-Myers Squibb for new trials. Operating costs rose to $133.1 million, resulting in a net loss of $108.6 million or $0.61 per share. The company is advancing its immuno-oncology pipeline despite challenges, with promising enrollment in key studies.
Nektar Therapeutics (NASDAQ:NKTR) presented additional clinical data from the Phase 1b study of NKTR-358, a T regulatory cell stimulator, at the ACR 2020 conference. The data showed NKTR-358 was safe and well-tolerated in patients with mild-to-moderate systemic lupus erythematosus (SLE), demonstrating a dose-dependent expansion of regulatory T cells and a reduction in clinical scores after three treatment cycles. The company is advancing to a Phase 2 trial in lupus patients, supported by encouraging biomarker changes, and is pursuing other studies in atopic dermatitis and psoriasis.
Nektar Therapeutics (NASDAQ: NKTR) will host a webcast conference call on November 4, 2020, at 4:15 p.m. EST, featuring insights on NKTR-358, their investigational therapy for autoimmune diseases, during the ACR 2020 event. Dr. David Klatzmann from Sorbonne University will discuss findings from their Phase 1b study. Additional details include a virtual poster presentation on November 9, 2020, showcasing data on regulatory T cells and NKTR-358's role in lupus treatment. A Phase 2 study for NKTR-358 is currently in progress.
Nektar Therapeutics (NKTR) will report its Q3 2020 financial results on November 5, 2020, after U.S. markets close. CEO Howard Robin will lead a conference call at 5:00 p.m. ET. The conference call details include the dial-in number: (877) 881-2183 for U.S. participants and (970) 315-0453 for international callers, with a conference ID of 5192707. The call will be accessible via a live webcast and available for replay until December 1, 2020. For more information, visit their website.
Nektar Therapeutics (NASDAQ: NKTR) has received FDA clearance for an Investigational New Drug application for bempegaldesleukin (BEMPEG, NKTR-214) in a Phase 1b study targeting mild COVID-19. The trial, starting in November, will assess BEMPEG's ability to enhance lymphocyte production, potentially improving treatment outcomes for COVID-19 patients. Key endpoints include changes in lymphocyte counts and clinical progression based on the WHO scale. The study aims to confirm BEMPEG's safety and tolerability while exploring its role in stimulating adaptive immune responses against COVID-19.
Vaccibody AS and Nektar Therapeutics (NKTR) have commenced a Phase 1/2a trial combining bempegaldesleukin (bempeg) with VB10.NEO, a personalized cancer vaccine, for advanced squamous cell carcinoma of the head and neck. The first patient has been dosed in this innovative study aimed at enhancing T cell responses to target tumors. Prior data indicated that VB10.NEO elicited responses in 50% of patients with various solid tumors, leading to optimism about combining it with bempeg. This collaboration aims to deepen the anti-tumor activity by leveraging both therapies' strengths.