Full Press Release Details
Therapeutics Reports Third Quarter 2024 Financial Results
FRANCISCO, November 7, 2024 /PRNewswire/ -- Nektar Therapeutics (Nasdaq: NKTR) today reported financial results for the third quarter
ended September 30, 2024.
and investments in marketable securities on September 30, 2024 were $249.0 million as compared to $329.4 million at December 31, 2023.
Nektar's cash and marketable securities are expected to support strategic development activities and operations into the fourth
"We made excellent progress this quarter advancing our I&I pipeline,
including the ongoing Phase 2b studies of rezpegaldesleukin in atopic dermatitis and alopecia areata," said Howard W. Robin, President
and CEO of Nektar. "We see rapid enrollment in the 400-patient atopic dermatitis study for rezpegaldesleukin, and we remain on track
for topline data in the first half of 2025. Our Phase 2 study in alopecia areata is also enrolling nicely with topline data expected in
the second half of 2025."
"Beyond rezpegaldesleukin, we are focused on advancing our earlier
stage TNFR2 antibody and bispecific programs, NKTR-0165 and NKTR-0166, with at least one of these slated to enter the clinic next year,"
continued Robin. "Next week, we are looking forward to presenting highly promising data at the 2024 ACR Convergence Meeting for
our preclinical PEG-CSF program, NKTR-422. Finally, we recently published important data for our IL-15 agonist, NKTR-255, highlighting
its potential as a validated mechanism in oncology."
of Financial Results
in the third quarter of 2024 was $24.1 million compared to the same $24.1 million in the third quarter of 2023. Revenue for the first
nine months of 2024 was $69.3 million compared to $66.2 million in the first nine months of 2023.
operating costs and expenses in the third quarter of 2024 were $58.5 million compared to $69.0 million in the third quarter of 2023.
Total operating costs and expenses in the first nine months of 2024 were $188.8 million compared to $296.4 million in the first nine
months of 2023. Operating costs and expenses for the first nine months of 2024 decreased primarily due to decreases in restructuring,
impairment and costs of terminated programs and a one-time $76.5 million non-cash goodwill impairment recognized in the first quarter
expense in the third quarter of 2024 was $35.0 million compared to $24.1 million for the third quarter of 2023. For the first nine months
of 2024, R&D expense was $92.2 million compared to $84.2 million in the first nine months of 2023. R&D expense increased for
both the third quarter and the first nine months of 2024 primarily due to increases in development expenses for rezpegaldesleukin and
NKTR-0165, partially offset by decreases in employee and related facilities costs, as well as development expenses for NKTR-255.
expense was $19.0 million in the third quarter of 2024 compared to $21.1 million in the third quarter of 2023. G&A expense was $59.6
million for the first nine months of 2024 compared to $60.1 million in the first nine months of 2023. G&A expense decreased for both
the third quarter and the first nine months of 2024 primarily due to decreases in employee costs, partially offset by the reduction of
facilities costs allocated to research and development expenses.
restructuring and impairment charges were less than $0.1 million in the third quarter of 2024 and $14.3 million in the first nine months
of 2024. These non-cash charges are related to the declining San Francisco commercial real estate market and real estate lease obligations
loss for the third quarter of 2024 was $37.1 million or $0.18 basic and diluted loss per share compared to a net loss of $45.8 million
or $0.24 basic and diluted loss per share in the third quarter of 2023. Net loss in the first nine months of 2024 was $126.2 million or $0.62 basic
and diluted loss per share compared to a net loss of $234.0 million or $1.23 basic and diluted loss per share
in the first nine months of 2023. Excluding the $14.3 million in non-cash restructuring and real estate impairment
charges, net loss, on a non-GAAP basis, for the first nine months of 2024 was $111.9 million, or $0.55 basic and diluted loss per
Quarter 2024 and Recent Business Highlights
also announced presentations at the following medical meetings:
Society for Immunotherapy of Cancer (SITC) Annual Meeting
Abstract (LBA) 1489: " REStoring lymphoCytes Using NKTR-255 after chemoradiothErapy in solid tumors (RESCUE): Preplanned Interim
Safety and Efficacy Analysis", Lin, S.
ePoster will be on display on the SITC 2024 virtual meeting platform on Thursday, November 7, 2024, at 9:00 a.m. CST
American College of Rheumatology (ACR) Convergence
1866120: "A Novel Therapeutically Active CSF-1R Agonist Promotes Tissue Macrophages Inflammation Resolution and Induces Tissue
Repair Pathways", Kivimae, S.
Presentation Type: Oral
Session: Abstracts: Cytokines & Cell Trafficking
Presentation Time: Monday, November 18 at 3:15 PM - 3:30 PM
American Society of Hematology (ASH) Annual Meeting
203576: "NKTR-255 Vs Placebo to Enhance Complete Responses and Durability Following CD19-Directed CAR-T Therapy in Patients with
Relapsed/Refractory (R/R) Large B-cell Lymphoma (LBCL)", Ahmed, S.
Presentation Type: Poster
Session: Cellular Immunotherapies: Early Phase Clinical Trials and Toxicities
Presentation Time: Saturday, December 7 at 5:30 PM - 7:30 PM
Call to Discuss Third Quarter 2024 Financial Results
management will host a conference call to review the results beginning at 5:00 p.m. Eastern Time/2:00 p.m. Pacific Time on November 7,
press release and live audio-only webcast of the conference call can be accessed through a link that is posted on the Home Page and Investors
section of the Nektar website: http://ir.nektar.com/. The web broadcast of the conference call will be available for replay through December
access the conference call, please pre-register at Nektar Earnings Call Registration. All registrants will receive dial-in information
and a PIN allowing them to access the live call.
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 and one in alopecia
areata. Our pipeline also includes a preclinical candidate NKTR-0165, which is a bivalent tumor necrosis factor receptor type II agonist
antibody. 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,
Note Regarding Forward-Looking Statements
press release contains forward-looking statements which can be identified by words such as: "will,"
"expect," "develop," "potential," "advance," "anticipate," 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, and whether all
the closing conditions of the announced definitive agreement will be met. 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) 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; (v) 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 (vi) certain other important risks and uncertainties set forth in our
Quarterly Report on Form 10-Q filed with the Securities and Exchange Commission on August 9, 2024. 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.
Wu of Nektar Therapeutics
LifeSci Communications
CONDENSED CONSOLIDATED BALANCE SHEETS
| September 30, 2024 | December 31, 2023 (1) | |||||||
| ASSETS | ||||||||
| Current assets: | ||||||||
| Cash and cash equivalents | $ | 30,109 | $ | 35,277 | ||||
| Short-term investments | 214,386 | 268,339 | ||||||
| Accounts receivable | - | 1,205 | ||||||
| Inventory, net | - | 16,101 | ||||||
| Other current assets | 8,933 | 9,779 | ||||||
| Assets held for sales | 33,053 | - | ||||||
| Total current assets | 286,481 | 330,701 | ||||||
| Long-term investments | 4,537 | 25,825 | ||||||
| Property, plant and equipment, net | 3,603 | 18,856 | ||||||
| Operating lease right-of-use assets | 8,826 | 18,007 | ||||||
| Other assets | 4,519 | 4,644 | ||||||
| Total assets | $ | 307,966 | $ | 398,033 | ||||
| LIABILITIES AND STOCKHOLDERS' EQUITY | ||||||||
| Current liabilities: | ||||||||
| Accounts payable | 8,577 | 9,848 | ||||||
| Accrued expenses | 32,377 | 22,162 | ||||||
| Operating lease liabilities, current portion | 21,504 | 19,259 | ||||||
| Liabilities related to assets held for sale | 5,125 | - | ||||||
| Total current liabilities | 67,583 | 51,269 | ||||||
| Operating lease liabilities, less current portion | 86,758 | 98,517 | ||||||
| Liabilities related to the sales of future royalties, net | 97,829 | 112,625 | ||||||
| Other long-term liabilities | 6,912 | 4,635 | ||||||
| Total liabilities | 259,082 | 267,046 | ||||||
| Commitments and contingencies | ||||||||
| Stockholders' equity: | ||||||||
| Preferred stock | - | - | ||||||
| Common stock | 19 | 19 | ||||||
| Capital in excess of par value | 3,654,981 | 3,608,137 | ||||||
| Treasury stock | (3,000 | ) | - | |||||
| Accumulated other comprehensive income (loss) | 355 | 80 | ||||||
| Accumulated deficit | (3,603,471 | ) | (3,477,249 | ) | ||||
| Total stockholders' equity | 48,884 | 130,987 | ||||||
| Total liabilities and stockholders' equity | $ | 307,966 | $ | 398,033 |