Cash and investments in marketable securities at December 31, 2021 were approximately
"We are pleased with the significant progress that Nektar has made advancing our clinical pipeline in 2021 in the areas of solid tumors, liquid tumors and auto-immune disorders," said
Summary of Financial Results
Revenue in the fourth quarter of 2021 was $25.0 million as compared to $23.5 million in the fourth quarter of 2020. Revenue for the year ended
Total operating costs and expenses in the fourth quarter of 2021 were
R&D expense in the fourth quarter of 2021 was
G&A expense was
Net loss for the fourth quarter of 2021 was $145.6 million or
2021 Business Highlights:
- In
December 2021 , Nektar announced Phase 1b proof-of-concept data for NKTR-358, a novel T regulatory cell stimulator, in patients with moderate-to-severe atopic dermatitis. The data demonstrate the potential for NKTR-358 to differentiate from standard of care and supports Eli Lilly's planned Phase 2 study in this indication. - In
December 2021 , Nektar presented data from the dose-escalation portion of its ongoing Phase 1 study of NKTR-255 in patients with relapsed/refractory hematologic malignancies at the 63rdAmerican Society of Hematology (ASH) Annual Meeting. The data supports the development of NKTR-255 in combination with anticancer agents that induce antibody dependent cellular toxicity as well as CAR-T therapies. - In
November 2021 , Nektar presented clinical data from the ongoing PROPEL study evaluating bempegaldesleukin plus KEYTRUDA® (pembrolizumab) in patients with non-small cell lung cancer at the 2021European Society for Medical Oncology Immuno-Oncology (ESMO-IO) Congress . - In
November 2021 , Nektar presented initial clinical results from the Phase 1/2 study of NKTR-255 in combination with cetuximab in solid tumors in a late-breaking abstract at the 2021Society for Immunotherapy of Cancer (SITC) Annual Meeting. The data showed early evidence of clinical benefit in the first patients treated in the dose-escalation portion of the study. - In
October 2021 , Bristol-Myers Squibb and Nektar completed enrollment in the Phase 3 first-line metastatic melanoma study evaluating bempegaldesleukin combined with Opdivo® versus Opdivo® in 760 patients with previously untreated, unresectable or metastatic melanoma. - In
September 2021 , Nektar entered into a new oncology clinical collaboration with Merck KGaA, Darmstadt,Germany and Pfizer Inc. to evaluate the maintenance regimen of NKTR-255 in combination with avelumab, a PD-L1 inhibitor, in patients with locally advanced or metastatic urothelial carcinoma (UC) in the Phase II JAVELIN Bladder Medley study. The study is expected to begin enrolling patients in the second quarter of 2022. - In
July 2021 , data from the Phase 2 study of bempegaldesleukin combined with Opdivo® was published in theJournal of Clinical Oncology , highlighting the encouraging safety and efficacy data in patients with first-line metastatic melanoma. - In
May 2021 , Nektar announced the publication of preclinical data in theJournal of Translational Autoimmunity describing NKTR-358 as a first-in-class, composition of stable PEG conjugates of native IL-2 designed to selectively stimulate T regulatory cell function. - In
May 2021 , Nektar announced its first publication of preclinical data highlighting anti-tumor properties of IL-15 agonist, NKTR-255, in theJournal for ImmunoTherapy of Cancer . - In
February 2021 , Nektar announced a clinical trial collaboration and supply agreement with Merck for a Phase 2/3 study of bempegaldesleukin in combination with KEYTRUDA® (pembrolizumab) for first-line treatment of patients with metastatic or unresectable recurrent squamous cell carcinoma of the head and neck (SCCHN) whose tumors express PD-L1. - In
February 2021 , Nektar announced a financing and co-development collaboration withSFJ Pharmaceuticals ® for the development of bempegaldesleukin plus KEYTRUDA® (pembrolizumab) in SCCHN. SFJ agreed to fund up to$150 million to support the planned Phase 2/3 study and to manage clinical trial operations for the study. In return, Nektar agreed to pay SFJ success-based annual milestone payments over a period of seven to eight years, which are contingent upon receipt of certainU.S. regulatory approvals for specified indications for bempegaldesleukin, and will begin following completion of the SCCHN study.
Conference Call to Discuss Fourth Quarter and Year-End 2021 Financial Results
Nektar management will host a conference call to review the results beginning at 5:00 p.m. Eastern Time/
This press release and a 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: https://ir.nektar.com/. The web broadcast of the conference call will be available for replay through March 28, 2022.
To access the conference call, follow these instructions:
Dial: (877) 881-2183 (
Conference ID: 8890486 (Nektar Therapeutics is the host)
In the event that any non-GAAP financial measure is discussed on the conference call that is not described in this press release, or explained on the conference call, related information will be made available on the Investors section of the Nektar website as soon as practical after the conclusion of the conference call.
About Nektar
Cautionary Note Regarding Forward-Looking Statements
This press release contains forward-looking statements which can be identified by words such as: "will," "may," "design," "potential," "initiate," "plan," "advance" and similar references to future periods. Examples of forward-looking statements include, among others, statements we make regarding the therapeutic potential of, and future development plans for, bempegaldesleukin, NKTR-358 and NKTR-255, the prospects and plans for our collaborations with other companies, and the timing of the initiation of clinical studies and the data readouts for our drug candidates. 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 bempegaldesleukin, NKTR-358 and NKTR-255 are based on preclinical and clinical findings and observations and are subject to change as research and development continue; (ii) bempegaldesleukin, NKTR-358 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 ongoing clinical studies (notwithstanding positive findings in earlier preclinical and clinical studies); (iii) bempegaldesleukin, NKTR-358 and NKTR-255 are in various stages of 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 November 5, 2021. 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.
Contact:
For Investors:
628-895-0661
For Media:
973-271-6085
dan@1abmedia.com
|
|||||||||||
CONDENSED CONSOLIDATED BALANCE SHEETS |
|||||||||||
(In thousands) |
|||||||||||
(Unaudited) |
|||||||||||
ASSETS |
|
|
(1) |
||||||||
Current assets: |
|||||||||||
Cash and cash equivalents |
$ 25,218 |
$ 198,955 |
|||||||||
Short-term investments |
708,737 |
862,941 |
|||||||||
Accounts receivable |
22,492 |
38,889 |
|||||||||
Inventory |
15,801 |
15,292 |
|||||||||
Other current assets |
23,333 |
21,928 |
|||||||||
Total current assets |
795,581 |
1,138,005 |
|||||||||
Long-term investments |
64,828 |
136,662 |
|||||||||
Property, plant and equipment, net |
60,510 |
59,662 |
|||||||||
Operating lease right-of-use assets |
117,025 |
126,476 |
|||||||||
|
76,501 |
76,501 |
|||||||||
Other assets |
2,744 |
1,461 |
|||||||||
Total assets |
$ 1,117,189 |
$ 1,538,767 |
|||||||||
LIABILITIES AND STOCKHOLDERS' EQUITY |
|||||||||||
Current liabilities: |
|||||||||||
Accounts payable |
9,747 |
22,139 |
|||||||||
Accrued compensation |
15,735 |
14,532 |
|||||||||
Accrued clinical trial expenses |
26,809 |
44,207 |
|||||||||
Other accrued expenses |
15,468 |
20,986 |
|||||||||
Operating lease liabilities, current portion |
17,441 |
13,915 |
|||||||||
Total current liabilities |
85,200 |
115,779 |
|||||||||
Operating lease liabilities, less current portion |
125,736 |
136,373 |
|||||||||
Development derivative liability |
27,726 |
- |
|||||||||
Liabilities related to the sales of future royalties, net |
195,427 |
200,340 |
|||||||||
Other long-term liabilities |
3,592 |
8,980 |
|||||||||
Total liabilities |
437,681 |
461,472 |
|||||||||
Commitments and contingencies |
|||||||||||
Stockholders' equity: |
|||||||||||
Preferred stock |
- |
- |
|||||||||
Common stock |
19 |
18 |
|||||||||
Capital in excess of par value |
3,516,641 |
3,388,730 |
|||||||||
Accumulated other comprehensive loss |
(4,157) |
(2,295) |
|||||||||
Accumulated deficit |
(2,832,995) |
(2,309,158) |
|||||||||
Total stockholders' equity |
679,508 |
1,077,295 |
|||||||||
Total liabilities and stockholders' equity |
$ 1,117,189 |
$ 1,538,767 |
|||||||||
(1) The consolidated balance sheet at |
|||||||||||
of the information and notes required by generally accepted accounting principles in |
|
||||||||||||||
CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS |
||||||||||||||
(In thousands, except per share information) |
||||||||||||||
(Unaudited) |
||||||||||||||
Three months ended |
Year ended |
|||||||||||||
2021 |
2020 |
2021 |
2020 |
|||||||||||
Revenue: |
||||||||||||||
Product sales |
$ 5,890 |
$ 2,884 |
$ 23,725 |
$ 17,504 |
||||||||||
Royalty revenue |
- |
(412) |
- |
30,999 |
||||||||||
Non-cash royalty revenue related to the sales of future royalties |
19,079 |
20,562 |
77,746 |
48,563 |
||||||||||
License, collaboration and other revenue |
40 |
428 |
436 |
55,849 |
||||||||||
Total revenue |
25,009 |
23,462 |
101,907 |
152,915 |
||||||||||
Operating costs and expenses: |
||||||||||||||
Cost of goods sold |
6,163 |
4,323 |
24,897 |
19,477 |
||||||||||
Research and development |
99,614 |
102,724 |
400,269 |
408,678 |
||||||||||
General and administrative |
32,142 |
27,136 |
122,844 |
104,682 |
||||||||||
Impairment of assets and other costs for terminated program |
- |
- |
- |
45,189 |
||||||||||
Total operating costs and expenses |
137,919 |
134,183 |
548,010 |
578,026 |
||||||||||
Loss from operations |
(112,910) |
(110,721) |
(446,103) |
(425,111) |
||||||||||
Non-operating income (expense): |
||||||||||||||
Change in fair value of development derivative liability |
(383) |
- |
(8,023) |
- |
||||||||||
Non-cash interest expense on liabilities related to the sales of future royalties |
(8,127) |
(8,183) |
(47,313) |
(30,267) |
||||||||||
Loss on revaluation of liability related to the sale of future royalties |
(24,410) |
- |
(24,410) |
- |
||||||||||
Interest income and other income (expense), net |
181 |
1,829 |
2,569 |
18,282 |
||||||||||
Interest expense |
- |
- |
- |
(6,851) |
||||||||||
Total non-operating expense, net |
(32,739) |
(6,354) |
(77,177) |
(18,836) |
||||||||||
Loss before provision for income taxes |
(145,649) |
(117,075) |
(523,280) |
(443,947) |
||||||||||
Provision for income taxes |
(4) |
128 |
557 |
493 |
||||||||||
Net loss |
$ (145,645) |
$ (117,203) |
$ (523,837) |
$ (444,440) |
||||||||||
Basic and diluted net loss per share |
$ (0.79) |
$ (0.65) |
$ (2.86) |
$ (2.49) |
||||||||||
Weighted average shares outstanding used in computing basic and diluted net loss per share |
184,964 |
179,684 |
183,298 |
178,581 |
|
||||||||||
CONDENSED CONSOLIDATED STATEMENTS OF CASH FLOWS |
||||||||||
(In thousands) |
||||||||||
(Unaudited) |
||||||||||
Year ended |
||||||||||
2021 |
2020 |
|||||||||
Cash flows from operating activities: |
||||||||||
Net loss |
$ (523,837) |
$ (444,440) |
||||||||
Adjustments to reconcile net loss to net cash used in operating activities: |
||||||||||
Non-cash royalty revenue related to the sales of future royalties |
(77,746) |
(48,563) |
||||||||
Non-cash interest expense on liabilities related to the sales of future royalties |
47,313 |
30,267 |
||||||||
Loss on revaluation of liability related to the sale of future royalties |
24,410 |
- |
||||||||
Change in fair value of development derivative liability |
8,023 |
- |
||||||||
Non-cash research and development expense |
16,703 |
- |
||||||||
Stock-based compensation |
94,674 |
94,261 |
||||||||
Depreciation and amortization |
14,146 |
14,182 |
||||||||
Impairment of advance payments to contract manufacturers and equipment for terminated program |
- |
20,351 |
||||||||
Amortization of premiums (discounts), net and other non-cash transactions |
6,730 |
3,943 |
||||||||
Changes in operating assets and liabilities: |
||||||||||
Accounts receivable |
12,397 |
1,913 |
||||||||
Inventory |
(509) |
(2,627) |
||||||||
Operating leases, net |
2,340 |
2,743 |
||||||||
Other assets |
(2,688) |
4,476 |
||||||||
Accounts payable |
(11,690) |
2,382 |
||||||||
Accrued compensation |
1,203 |
4,697 |
||||||||
Other accrued expenses |
(23,524) |
8,644 |
||||||||
Deferred revenue |
(605) |
(5,516) |
||||||||
Net cash used in operating activities |
(412,660) |
(313,287) |
||||||||
Cash flows from investing activities: |
||||||||||
Purchases of investments |
(960,689) |
(987,533) |
||||||||
Maturities of investments |
1,166,951 |
1,449,304 |
||||||||
Sales of investments |
11,504 |
41,700 |
||||||||
Purchases of property, plant and equipment |
(14,989) |
(7,258) |
||||||||
Net cash provided by investing activities |
202,777 |
496,213 |
||||||||
Cash flows from financing activities: |
||||||||||
Proceeds from sale of future royalties, net of |
- |
146,250 |
||||||||
Repayment of senior notes |
- |
(250,000) |
||||||||
Cash receipts from development derivative liability |
3,000 |
- |
||||||||
Proceeds from shares issued under equity compensation plans |
33,238 |
23,396 |
||||||||
Net cash provided by (used in) financing activities |
36,238 |
(80,354) |
||||||||
Effect of foreign exchange rates on cash and cash equivalents |
(92) |
20 |
||||||||
Net increase (decrease) in cash and cash equivalents |
(173,737) |
102,592 |
||||||||
Cash and cash equivalents at beginning of year |
198,955 |
96,363 |
||||||||
Cash and cash equivalents at end of year |
$ 25,218 |
$ 198,955 |
||||||||
Supplemental disclosure of cash flow information: |
||||||||||
Cash paid for interest |
$ - |
$ 9,742 |
||||||||
Cash paid for income taxes |
$ 325 |
$ 539 |
||||||||
Operating lease right-of-use assets recognized in exchange for lease liabilities |
$ 1,057 |
$ 2,133 |
||||||||
Accounts receivable recognized in exchange for long-term liabilities |
$ - |
$ 4,000 |
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