Puma Biotechnology Reports First Quarter 2021 Financial Results
Puma Biotechnology (PBYI) reported Q1 2021 financial results, with net NERLYNX revenue at $45.8 million, down from $48.6 million in Q1 2020. GAAP net income reached $16.5 million, marking a turnaround from a loss of $16.9 million the previous year. Total revenue was $98.2 million, bolstered by a $50 million licensing deal for NERLYNX in Greater China. Operating costs rose to $78 million, influenced by a one-time $20 million termination fee. Cash and marketable securities increased to $109.1 million. The company anticipates significant clinical milestones throughout 2021.
- GAAP net income of $16.5 million in Q1 2021, a turnaround from a net loss of $16.9 million in Q1 2020.
- Total revenue of $98.2 million, including a $50 million licensing agreement with Pierre Fabre.
- Increased cash and marketable securities to $109.1 million.
- Net NERLYNX revenue decreased by $2.8 million compared to Q1 2020.
- Total operating costs rose to $78 million, up from $65.5 million year-on-year, driven by a $20 million termination fee.
Puma Biotechnology, Inc. (NASDAQ: PBYI), a biopharmaceutical company, announced financial results for the first quarter ended March 31, 2021. Unless otherwise stated, all comparisons are for the first quarter of 2021 compared to the first quarter of 2020.
Product revenue, net consists entirely of sales revenue from NERLYNX®, Puma’s first commercial product. Net NERLYNX revenue in the first quarter of 2021 was
Based on accounting principles generally accepted in the United States (GAAP), Puma reported net income of
Non-GAAP adjusted net income was
Net cash provided by operating activities for the first quarter of 2021 was
“During the first quarter, we continued to face the challenges brought about by the COVID-19 pandemic and the reduction in commercial access caused by it,” said Alan H. Auerbach, Chairman, Chief Executive Officer and President of Puma. “We are hopeful that with the progress made with vaccinations, commercial access will improve in 2021 which will greatly aid our commercial abilities. We continue to remain focused on and committed to providing support to patients battling cancer.”
“In terms of clinical development, we are pleased that during the first quarter we were able to achieve the completion of enrollment in the randomized cohorts of the Phase II SUMMIT trial of neratinib for patients with hormone receptor-positive breast cancer that has a HER2 mutation. Enrollment in the other cohorts in SUMMIT continued as well, including for patients with EGFR exon 18 mutated non-small cell lung cancer and HER2 mutated cervical cancer. Additionally, our global partners continued to launch NERLYNX in several new countries during the first quarter and we look forward to launches in additional countries throughout 2021.”
Mr. Auerbach added, “We anticipate the following key milestones over the next 12 months: (i) reporting top line data from the randomized cohort of the Phase II SUMMIT trial of neratinib in hormone receptor positive breast cancer that has a HER2 mutation (2021); (ii) reporting Phase II data from the SUMMIT trial of neratinib in non-small cell lung cancer patients with EGFR exon 18 mutations (H2-2021); (iii) conducting a pre-NDA meeting with the FDA to discuss accelerated approval of neratinib in HER2-mutated hormone receptor positive breast cancer and HER2-mutated cervical cancer (2021); (iv) reporting data from the Phase II TBCRC-022 trial of the combination of Kadcyla plus neratinib in patients with HER2-positive breast cancer with brain metastases who have previously been treated with Kadcyla (H2-2021); (v) conducting a meeting with the FDA to discuss the potential for an accelerated approval pathway for neratinib in non-small cell lung cancer patients with EGFR exon 18 mutations who have previously been treated with an EGFR tyrosine kinase inhibitor (2021); and (vi) receiving regulatory decisions for the extended adjuvant HER2-positive early stage breast cancer indication in additional countries (2021).”
Revenue
Total revenue consists of product revenue, net from sales of NERLYNX, Puma’s first commercial product, license revenue from Puma’s sub-licensees and royalty revenue. For the first quarter ended March 31, 2021, total revenue was
Operating Costs and Expenses
Total operating costs and expenses were
Cost of Sales
Cost of sales was
Selling, General and Administrative Expenses
Selling, general and administrative expenses were
Research and Development Expenses
Research and development expenses were
Total Other Expenses
Total other expenses were
Conference Call
Puma Biotechnology will host a conference call to discuss its first quarter 2021 financial results and provide an update on the Company’s business and outlook at 1:30 p.m. PDT/4:30 p.m. EDT on Thursday, May 6, 2021. The call may be accessed by dialing 1-877-709-8150 (domestic) or 1-201-689-8354 (international). Please dial in at least 10 minutes in advance and inform the operator that you would like to join the “Puma Biotechnology Conference Call.” A live webcast of the conference call and presentation slides may be accessed on the Investors section of the Puma Biotechnology website at http://www.pumabiotechnology.com. A replay of the call will be available shortly after completion of the call and will be archived on Puma’s website for 90 days.
About Puma Biotechnology
Puma Biotechnology, Inc. is a biopharmaceutical company with a focus on the development and commercialization of innovative products to enhance cancer care. Puma in-licenses the global development and commercialization rights to PB272 (neratinib, oral), PB272 (neratinib, intravenous) and PB357. Neratinib, oral was approved by the U.S. Food and Drug Administration in 2017 for the extended adjuvant treatment of adult patients with early stage HER2-overexpressed/amplified breast cancer, following adjuvant trastuzumab-based therapy, and is marketed in the United States as NERLYNX® (neratinib) tablets. In February 2020, NERLYNX was also approved by the FDA in combination with capecitabine for the treatment of adult patients with advanced or metastatic HER2-positive breast cancer who have received two or more prior anti-HER2-based regimens in the metastatic setting. NERLYNX was granted marketing authorization by the European Commission in 2018 for the extended adjuvant treatment of adult patients with early stage hormone receptor-positive HER2-overexpressed/amplified breast cancer and who are less than one year from completion of prior adjuvant trastuzumab-based therapy. NERLYNX is a registered trademark of Puma Biotechnology, Inc.
Further information about Puma Biotechnology can be found at www.pumabiotechnology.com.
IMPORTANT SAFETY INFORMATION
NERLYNX® (neratinib) tablets, for oral use
INDICATIONS AND USAGE: NERLYNX is a kinase inhibitor indicated:
- As a single agent, for the extended adjuvant treatment of adult patients with early-stage HER2-positive breast cancer, to follow adjuvant trastuzumab-based therapy.
- In combination with capecitabine, for the treatment of adult patients with advanced or metastatic HER2-positive breast cancer, who have received two or more prior anti-HER2 based regimens in the metastatic setting.
CONTRAINDICATIONS: None
WARNINGS AND PRECAUTIONS:
- Diarrhea: Aggressively manage diarrhea. If diarrhea occurs despite recommended prophylaxis, treat with additional antidiarrheals, fluids, and electrolytes as clinically indicated. Withhold NERLYNX in patients experiencing severe and/or persistent diarrhea. Permanently discontinue NERLYNX in patients experiencing Grade 4 diarrhea or Grade ≥ 2 diarrhea that occurs after maximal dose reduction.
- Hepatotoxicity: Monitor liver function tests monthly for the first 3 months of treatment, then every 3 months while on treatment and as clinically indicated. Withhold NERLYNX in patients experiencing Grade 3 liver abnormalities and permanently discontinue NERLYNX in patients experiencing Grade 4 liver abnormalities.
- Embryo-Fetal Toxicity: NERLYNX can cause fetal harm. Advise patients of potential risk to a fetus and to use effective contraception.
ADVERSE REACTIONS:
The most common adverse reactions (reported in ≥
- NERLYNX as a single agent: Diarrhea, nausea, abdominal pain, fatigue, vomiting, rash, stomatitis, decreased appetite, muscle spasms, dyspepsia, AST or ALT increased, nail disorder, dry skin, abdominal distention, epistaxis, weight decreased, and urinary tract infection.
- NERLYNX in combination with capecitabine: Diarrhea, nausea, vomiting, decreased appetite, constipation, fatigue/asthenia, weight decreased, dizziness, back pain, arthralgia, urinary tract infection, upper respiratory tract infection, abdominal distention, renal impairment, and muscle spasms.
To report SUSPECTED ADVERSE REACTIONS, contact Puma Biotechnology, Inc. at 1-844-NERLYNX (1-844-637-5969) or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.
DRUG INTERACTIONS:
- Gastric acid reducing agents: Avoid concomitant use with proton pump inhibitors. When patients require gastric acid reducing agents, use an H2-receptor antagonist or antacid. Separate NERLYNX by at least 3 hours with antacids. Separate NERLYNX by at least 2 hours before or 10 hours after H2-receptor antagonists.
- Strong CYP3A4 inhibitors: Avoid concomitant use.
- Moderate CYP3A4 and P-glycoprotein (P-gp) dual inhibitors: Avoid concomitant use.
- Strong or moderate CYP3A4 inducers: Avoid concomitant use.
- P-glycoprotein (P-gp) substrates: Monitor for adverse reactions of narrow therapeutic agents that are P-gp substrates when used concomitantly with NERLYNX.
USE IN SPECIFIC POPULATIONS:
- Lactation: Advise women not to breastfeed.
Please see Full Prescribing Information for additional safety information.
To help ensure patients have access to NERLYNX, Puma has implemented the Puma Patient Lynx support program to assist patients and healthcare providers with reimbursement support and referrals to resources that can help with financial assistance. More information on the Puma Patient Lynx program can be found at www.NERLYNX.com or 1-855-816-5421.
Forward-Looking Statements
This press release contains forward-looking statements, including statements regarding the worldwide expansion of NERLYNX and Puma’s anticipated milestones. All forward-looking statements involve risks and uncertainties that could cause Puma’s actual results to differ materially from the anticipated results and expectations expressed in these forward-looking statements. These statements are based on current expectations, forecasts and assumptions, and actual outcomes and results could differ materially from these statements due to a number of factors, which include, but are not limited to, any adverse impact on Puma’s business or the global economy and financial markets, generally, from the global COVID-19 pandemic, and the risk factors disclosed in the periodic and current reports filed by Puma with the Securities and Exchange Commission from time to time, including Puma’s Annual Report on Form 10-K for the year ended December 31, 2020. Readers are cautioned not to place undue reliance on these forward-looking statements, which speak only as of the date hereof. Puma assumes no obligation to update these forward-looking statements, except as required by law.
| PUMA BIOTECHNOLOGY, INC. AND SUBSIDIARIES | ||||||||
| CONSOLIDATED STATEMENTS OF OPERATIONS | ||||||||
| (in millions except share and per share data) | ||||||||
| Three Months Ended | ||||||||
| March 31, | ||||||||
|
2021 |
|
|
2020 |
|
|||
| (Unaudited) | (Unaudited) | |||||||
| Revenues: | ||||||||
| Product revenue, net | $ |
45.8 |
|
$ |
48.6 |
|
||
| License revenue |
|
50.0 |
|
|
2.0 |
|
||
| Royalty revenue |
|
2.4 |
|
|
0.6 |
|
||
| Total revenue |
|
98.2 |
|
|
51.2 |
|
||
| Operating costs and expenses: | ||||||||
| Cost of sales |
|
29.6 |
|
|
9.1 |
|
||
| Selling, general and administrative |
|
28.2 |
|
|
30.9 |
|
||
| Research and development |
|
20.2 |
|
|
25.5 |
|
||
| Total operating costs and expenses |
|
78.0 |
|
|
65.5 |
|
||
| Income (loss) from operations |
|
20.2 |
|
|
(14.3 |
) |
||
| Other income (expenses): | ||||||||
| Interest income |
|
— |
|
|
0.4 |
|
||
| Interest expense |
|
(3.5 |
) |
|
(3.0 |
) |
||
| Legal verdict expense |
|
(0.2 |
) |
|
(0.1 |
) |
||
| Other income |
|
— |
|
|
0.1 |
|
||
| Total other expenses |
|
(3.7 |
) |
|
(2.6 |
) |
||
| Net income (loss) before income taxes |
|
16.5 |
|
|
(16.9 |
) |
||
| Income tax expense |
|
— |
|
|
— |
|
||
| Net income (loss) | $ |
16.5 |
|
$ |
(16.9 |
) |
||
| Net income (loss) per share of common stock—basic | $ |
0.41 |
|
$ |
(0.43 |
) |
||
| Net income (loss) per share of common stock—diluted | $ |
0.40 |
|
$ |
(0.43 |
) |
||
| Weighted-average shares of common stock outstanding—basic |
|
40,260,864 |
|
|
39,291,162 |
|
||
| Weighted-average shares of common stock outstanding—diluted |
|
40,894,868 |
|
|
39,291,162 |
|
||
| PUMA BIOTECHNOLOGY, INC. AND SUBSIDIARIES | ||||||||
| LIQUIDITY AND CAPITAL RESOURCES | ||||||||
| (in millions) | ||||||||
March 31, |
|
December 31, |
||||||
2021 |
|
2020 |
||||||
| (Unaudited) | ||||||||
| Cash and cash equivalents | $ |
95.7 |
|
$ |
85.3 |
|
||
| Marketable securities |
|
13.4 |
|
|
8.1 |
|
||
| Working capital |
|
23.4 |
|
|
31.9 |
|
||
| Stockholders' equity (deficit) |
|
16.4 |
|
|
(6.0 |
) |
||
| Three Months | Three Months | |||||||
| Ended | Ended | |||||||
| March 31, | March 31, | |||||||
2021 |
2020 |
|||||||
| (Unaudited) | (Unaudited) | |||||||
| Cash provided by (used in): | ||||||||
| Operating activities | $ |
15.7 |
|
$ |
(11.5 |
) |
||
| Investing activities |
|
(5.3 |
) |
|
34.3 |
|
||
| Financing activities |
|
— |
|
|
— |
|
||
| Increase (decrease) in cash and cash equivalents, and restricted cash | $ |
10.4 |
|
$ |
22.8 |
|
||
Use of Non-GAAP Measures
In addition to operating results as calculated in accordance with GAAP, Puma uses certain non-GAAP financial measures when planning, monitoring, and evaluating operational performance. The following table presents the Company’s net income (loss) and net income (loss) per share calculated in accordance with GAAP and as adjusted to remove the impact of stock-based compensation. For the three months ended March 31, 2021 and 2020, stock-based compensation represented approximately
| PUMA BIOTECHNOLOGY, INC. AND SUBSIDIARIES | |||||||||
| Reconciliation of GAAP Net Income (Loss) to Non-GAAP Adjusted Net Income (Loss) and | |||||||||
| GAAP Net Income (Loss) Per Share to Non-GAAP Adjusted Net Income (Loss) Per Share | |||||||||
| (in millions except share and per share data) | |||||||||
| (Unaudited) | |||||||||
| Three Months Ended March 31, | |||||||||
2021 |
2020 |
||||||||
| GAAP net income (loss) | $ |
16.5 |
$ |
(16.9 |
) |
||||
| Adjustments: | |||||||||
| Stock-based compensation - | |||||||||
| Selling, general and administrative |
|
3.6 |
|
4.7 |
|
(1) |
|||
| Research and development |
|
2.3 |
|
4.2 |
|
(2) |
|||
| Non-GAAP adjusted net income (loss) | $ |
22.4 |
$ |
(8.0 |
) |
||||
| GAAP net income (loss) per share—basic | $ |
0.41 |
$ |
(0.43 |
) |
||||
| Adjustment to net income (loss) (as detailed above) |
|
0.15 |
|
0.23 |
|
||||
| Non-GAAP adjusted basic net income (loss) per share | $ |
0.56 |
$ |
(0.20 |
) |
(3) |
|||
| GAAP net income (loss) per share—diluted | $ |
0.40 |
$ |
(0.43 |
) |
||||
| Adjustment to net income (loss) (as detailed above) |
|
0.15 |
|
0.23 |
|
||||
| Non-GAAP adjusted diluted net income (loss) per share | $ |
0.55 |
(4) |
$ |
(0.20 |
) |
(5) |
||
| (1) To reflect a non-cash charge to operating expense for selling, general, and administrative stock-based compensation. | ||||||||
| (2) To reflect a non-cash charge to operating expense for research and development stock-based compensation. | ||||||||
| (3) Non-GAAP adjusted basic net income (loss) per share was calculated based on 40,260,864 and 39,291,162 weighted-average shares of common stock outstanding for the three months ended March 31, 2021 and 2020, respectively. | ||||||||
| (4) Non-GAAP adjusted diluted net income per share was calculated based on 40,894,868 weighted-average shares of common stock outstanding for the three months ended March 31, 2021. | ||||||||
| (5) Potentially dilutive common stock equivalents (stock options, restricted stock units and warrants) were not included in this non-GAAP adjusted diluted net loss per share for the three months ended March 31, 2020, as these shares would be considered anti-dilutive. |
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FAQ
What were Puma Biotechnology's Q1 2021 earnings per share (EPS)?
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