Puma Biotechnology Reports Third Quarter 2013 Financial Results

Puma Biotechnology Reports Third Quarter 2013

LOS ANGELES, Calif.,

Nov. 12, 2013 Puma Biotechnology, Inc. (NYSE: PBYI), a development stage biopharmaceutical company, today announced financial results for the third quarter ended September 30, 2013.

Unless otherwise stated, all comparisons are for the third quarter and nine months ended September 30, 2013, compared to the third quarter and nine

months ended September 30, 2012.

Based on accounting principles generally accepted in the United States (GAAP), Puma reported a net loss applicable

to common stock of $14.3 million, or $0.50 per share, for the third quarter of 2013, compared to a net loss of $25.9 million, or $1.29 per share, for the third quarter of 2012. Net loss applicable to common stock for the nine months ended

September 30, 2013, was $38.7 million, or $1.35 per share, compared to $52.4 million, or $2.62 per share, for the nine months ended September 30, 2012.

Adjusted net loss applicable to common stock was $12.3 million, or $0.43 per share, for the third quarter of 2013, compared to adjusted net loss applicable to

common stock of $3.6 million, or $0.18 per share, for the third quarter of 2012. Adjusted net loss applicable to common stock for the nine months ended September 30, 2013, was $33.6 million, or $1.17 per share, compared to $11.5 million, or

$0.58 per share, for the nine months ended September 30, 2012. Adjusted net loss applicable to common stock excludes stock-based compensation expense and external costs associated with ongoing clinical trials of our lead product candidate,

PB272 (neratinib (oral)), that Puma assumed from a licensor and which it refers to as licensor legacy clinical trials. For a reconciliation of adjusted net loss applicable to common stock to reported net loss applicable to common stock, please see

the financial tables at the end of this news release.

Net cash used in operating activities for the third quarter of 2013 was $12.0 million. Net cash

used in operating activities for the nine months ended September 30, 2013, was $41.4 million. At September 30, 2013, Puma had cash and cash equivalents of $51.3 million and marketable securities of $44.4 million, compared to $137.4 million

of cash and cash equivalents at December 31, 2012. As previously noted, Puma s license agreement for PB272 established a limit on the Company s expenses related to certain clinical trials Puma assumed from the licensor, or legacy

clinical trials. Puma reached this limit, or cap, during the fourth quarter of 2012; therefore, the licensor is responsible for expenses related to the legacy clinical trials until such trials are completed. The license agreement requires the

Company to bill the licensor quarterly for external out-of-pocket costs in excess of the cap cost. At September 30, 2013, the Company reported a receivable of approximately $11.3 million associated with outstanding invoices to the

licensor. The Company anticipates receiving payments for these outstanding invoices by the end of 2013.

During the third quarter of 2013, we

continued to execute on our ongoing Phase II and Phase III trials of PB272 (neratinib), said Alan H. Auerbach, Chief Executive Officer and President of Puma. During the quarter, we also initiated a Phase II trial of PB272 for the

treatment of patients with solid tumors that have a HER2 activating mutation (basket trial). We anticipate seeing the first results from our basket trial in the fourth quarter of 2013 or in the beginning of 2014.

In addition, noted Mr. Auerbach, we expect to (i) complete the ongoing Phase II clinical trial of PB272 in combination with

temsirolimus in fourth-line HER2-positive metastatic breast cancer, which we anticipate

reporting additional data from later in 2013 or in early 2014; (ii) initiate a Phase III trial of the combination of PB272 plus temsirolimus in the first half of 2014; (iii) complete

the ongoing Phase II trial of PB272 in patients with HER2-positive metastatic breast cancer that has metastasized to the brain, which we anticipate reporting data from later in 2013 or in early 2014; (iv) complete our two ongoing Phase II

trials of PB272 as a neoadjuvant treatment for patients with HER2-positive breast cancer (I-SPY2 and NSABP FB-7), both of which we expect to report data from in the fourth quarter of 2013; (v) report data from our Phase II trial of PB272 in

patients with HER2 mutated non-small cell lung cancer later in 2013; (vi) continue our Phase II trial of PB272 in HER2-negative breast cancer patients who have a HER2 mutation, which we also have the potential to report initial data from later

in 2013; (vii) complete our ongoing Phase II randomized trial of PB272 as a first-line treatment for HER2-positive metastatic breast cancer, which we expect to report data from in the first half of 2014; and (viii) complete our Phase III

trial of PB272 as an adjuvant treatment for HER2 positive breast cancer, which we expect to report data from in the first half of 2014.

Based on GAAP, operating expenses

were $14.3 million for the third quarter of 2013, compared to $25.9 million for the third quarter of 2012. Operating expenses for the nine months ended September 30, 2013, were $38.8 million, compared to $52.5 million for the nine months ended

Adjusted operating expenses were $12.3 million for the third quarter of 2013, compared to $3.6 million in the third quarter of

2012. Adjusted operating expenses exclude stock-based compensation expenses and licensor legacy clinical trial costs. Adjusted operating expenses for the nine months ended September 30, 2013, were $33.7 million, compared to $11.6 million for

the nine months ended September 30, 2012. For a reconciliation of adjusted operating expenses to reported operating expenses, please see the financial tables at the end of this news release.

General and Administrative Expenses:

general and administrative expenses were $2.3 million in the third quarter of 2013, compared to $8.1 million in the third quarter of 2012. General and administrative expenses for the nine months ended September 30, 2013, were $6.8 million

compared to $11.1 million for the nine months ended September 30, 2012.

Adjusted general and administrative expenses were $1.8 million for the third

quarter of 2013, compared to $1.5 million in the third quarter of 2012. Adjusted general and administrative expenses for the nine months ended September 30, 2013, were $5.4 million, compared to $4.6 million for the nine months ended

Research and Development Expenses:

Based on GAAP, research and development expenses were $12.0 million in the third quarter of 2013, compared to $17.8 million in the third quarter of 2012.

Research and development expenses for the nine months ended September 30, 2013, were $32.0 million, compared to $41.4 million for the nine months ended September 30, 2012.

Adjusted research and development expenses were $10.5 million in the third quarter of 2013, compared to $2.1 million in the third quarter of 2012. The

increase in adjusted research and development expenses from the third quarter of 2012 was driven primarily by costs associated with the initiation of Puma-sponsored clinical trials and the testing and validation of the active pharmaceutical

ingredient of our lead drug candidate. Adjusted research and development expenses for the nine months ended September 30, 2013, were $28.3 million, compared to $7.0 million for the nine months ended September 30, 2012.

About Puma Biotechnology

Puma Biotechnology, Inc. is a development stage biopharmaceutical company that acquires and develops innovative products for the treatment of various forms of

cancer. The Company focuses on in-licensing drug candidates that are undergoing or have already completed initial clinical testing for the treatment of cancer and then seeks to further develop those drug candidates for commercial use. The Company is

initially focused on the development of PB272 (oral neratinib), a potent irreversible tyrosine kinase inhibitor, for the treatment of patients with HER2-positive metastatic breast cancer and patients with non-small cell lung cancer, breast cancer

and other solid tumors that have a HER2 mutation.

Further information about Puma Biotechnology can be found at www.pumabiotechnology.com.

Forward-Looking Statements:

This press release contains

forward-looking statements, including statements regarding anticipated timing for the commencement and completion of various clinical trials and the announcement of data relative to these trials. All forward-looking statements included in this press

release involve risks and uncertainties that could cause the Company 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, the fact that the Company has no product revenue and no

products approved for marketing, the Company s dependence on PB272, which is still under development and may never receive regulatory approval, the challenges associated with conducting and enrolling clinical trials, the risk that the results

of clinical trials may not support the Company s drug candidate claims, even if approved, the risk that physicians and patients may not accept or use the Company s products, the Company s reliance on third parties to conduct its

clinical trials and to formulate and manufacture its drug candidates, the Company s dependence on licensed intellectual property, and the other risk factors disclosed in the periodic reports filed by the Company with the Securities and Exchange

Commission from time to time, including the Company s Annual Report on Form 10-K for the year ended December 31, 2012. Readers are cautioned not to place undue reliance on these forward-looking statements, which speak only as of the date

hereof. The Company assumes no obligation to update these forward-looking statements, except as required by law.

Alan H. Auerbach or Mariann Ohanesian, Puma Biotechnology, Inc., +1 424 248 6500

Andreas Marathovouniotis or David Schull, Russo Partners, +1 212 845 4235

(Financial Tables Follow)

PUMA BIOTECHNOLOGY, INC. AND SUBSIDIARY

(A DEVELOPMENT STAGE COMPANY)

CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS

except per share data)

PUMA BIOTECHNOLOGY, INC.

(A DEVELOPMENT STAGE COMPANY)

LIQUIDITY AND CAPITAL RESOURCES

(in millions except per share data)

Reconciliation of GAAP and Non-GAAP Financial Information

(in millions except share and per share data)