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Share Name | Share Symbol | Market | Type |
---|---|---|---|
Avid Bioservices Inc | NASDAQ:CDMO | NASDAQ | Common Stock |
Price Change | % Change | Share Price | Bid Price | Offer Price | High Price | Low Price | Open Price | Shares Traded | Last Trade | |
---|---|---|---|---|---|---|---|---|---|---|
0.04 | 0.52% | 7.67 | 7.19 | 8.10 | 7.85 | 7.465 | 7.61 | 1,527,702 | 01:00:00 |
-- Avid Achieves Year-Over-Year Topline Revenue Growth of 30% Exceeding $57 Million --
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Highlights Since January 31, 2017“We are very pleased to announce that the business recorded its highest annual revenue to date during fiscal 2017,” stated Steven W. King, president and chief executive officer of Peregrine, and president of Avid Bioservices. “While we are happy to report continued year-over-year revenue growth, we are projecting revenues for FY 2018 to be similar with FY 2017 due to recent changes in the forecast of a large customer and a delayed regulatory filing for another customer. We believe this is a temporary lull and remain confident that Avid is in a strong position for continued growth in the future.” Mr. King continued, “An important part of continuing revenue growth and reducing risk for the business is to attract new customers. On that front, we have recently signed four new customers that we expect to contribute to top-line revenue in FY 2018 and into the future. In addition, we successfully completed three process validation campaigns this fiscal year for existing third-party customers which we believe may significantly contribute to future revenue as these customers move toward building inventory for their potential launch, and commercial supply.
“We are also continuing to take other important steps to ensure Avid’s growth in the coming years. As part of this effort, we have recently installed two new 2,000 liter bioreactors in our Myford facility, and we already have commitments for part of this capacity. Due to its state-of-the-art and modular design, there remains potential to install additional bioreactors in Myford, which will allow us to continue growing the business within our current facilities.
“Turning to the Peregrine business, we were able to generate some of the most compelling bavituximab data to date, further supporting the combination of bavituximab and checkpoint inhibitors even while reducing R&D spending by over 50% in FY 2017. The clinical findings came from the comprehensive analysis of maturing Phase III SUNRISE data while impressive preclinical results came from our collaborators at Memorial Sloan Kettering Cancer Center (MSKCC). The researchers at MSKCC presented promising preclinical data combining PS-targeting with adoptive T cell transfer therapy which may support the combination of bavituximab with CAR-T cell immunotherapy in the future.
“Both Peregrine and Avid have achieved important milestones in recent quarters. The success of Avid and its continued revenue growth with the compelling data we have seen from the Phase III SUNRISE trial have led us to explore various strategic options that we believe will enable us to enhance stockholder value for all stockholders, including the possible separation of these two distinct businesses.”
Research and Development Highlights"The most compelling data to date from the Phase III SUNRISE trial was presented at AACR and together with the PD-L1 results presented at ASCO this year add to the growing body of data supporting the further development of bavituximab with checkpoint inhibitors," said Joseph Shan, vice president of clinical and regulatory affairs at Peregrine.
AACR Highlights: In a subgroup analysis, Peregrine researchers looked at the outcome of 91 patients that were enrolled in the Phase III SUNRISE trial that were subsequently treated with anti-PD-1/PD-L1 immune checkpoint inhibitors (“ICI’s”) post study treatments. The results from this analysis demonstrated that the patients who received docetaxel plus bavituximab (Doc+Bavi) and subsequent ICI had not yet reached median overall survival (“mOS”) compared to mOS of 13.0 months for patients who received docetaxel plus placebo (Doc+Placebo) (hazard ratio [HR], 0.43; p=0.005). The statistically significant difference between the two arms in the trial provides strong rationale for combining bavituximab with ICI’s and supports the hypothesis that bavituximab may modulate the tumor microenvironment to enhance the anti-tumor activity of ICI’s.
A photo accompanying this announcement is available at http://www.globenewswire.com/NewsRoom/AttachmentNg/428c1a61-a599-4976-8a92-d65148671bcd
ASCO Highlights:Peregrine researchers presented additional supportive data demonstrating that patients in the bavituximab containing arm who had low baseline PD-L1 expression on tumor cells (i.e., patients typically with poorer response to PD-1/PD-L1 checkpoint inhibitors) lived significantly longer than patients with high baseline PD-L1 expression. These data further support the hypothesis that bavituximab may modulate the tumor microenvironment to complement and enhance the anti-tumor activity of ICI’s.
NCCN Highlights:The three clinical trials under the collaboration with the NCCN are advancing as planned.
Preclinical Highlights:Researchers from Memorial Sloan Kettering Cancer Center (MSKCC) presented a preclinical study evaluating the anti-tumor activity and toxicities of adoptive T cell transfer therapy in combination with either PS-targeting antibodies or anti-OX40 antibodies in mice with advanced melanomas. Whereas PS-targeting and anti-OX40 demonstrated comparable tumor regression when administered in combination with transferred adoptive T cells, only the PS-targeting combination achieved these results without any off-target toxicities. In contrast, the anti-OX40 treatment combination triggered off-target side effects.
PS Exosome Technology Highlights:The company continues to make progress with its PS exosome diagnostic technology that is designed to detect and monitor cancer. The assay has been successfully optimized and we are currently preparing to generate additional data by testing human samples. Such data will be important to partnering discussions.
Avid Bioservices Highlights"FY 2017 was a strong year for Avid Bioservices with year-over-year revenue growth of 30% compared to FY 2016. The company recognized revenue of $17.9 million for the fourth quarter and $57.6 million for the full fiscal year,” stated Paul Lytle, chief financial officer of Peregrine. "While we missed our revenue guidance of $60 to $65 million, we were ready to ship a number of process validation runs which were delayed due to events outside our control. This delay has caused approximately $10 million in manufacturing revenue to shift from fiscal year 2017 to fiscal year 2018.”
Financial Highlights and Results
More detailed financial information and analysis may be found in Peregrine's Annual Report on Form 10-K, which will be filed with the Securities and Exchange Commission today.
Conference CallPeregrine will host a conference call and webcast this afternoon, July 14, 2017, at 4:30 PM EDT (1:30 PM PDT).
To listen to the conference call, please dial (877) 312-5443 or (253) 237-1126 and request the Peregrine Pharmaceuticals conference call. To listen to the live webcast, or access the archived webcast, please visit: http://ir.peregrineinc.com/events.cfm.
About Peregrine Pharmaceuticals, Inc.Peregrine Pharmaceuticals, Inc. is a biopharmaceutical company committed to improving the lives of patients by delivering high quality pharmaceutical products through its contract development and manufacturing organization (CDMO) services and through advancing and licensing its investigational immunotherapy and related products. Peregrine's in-house CDMO services, including cGMP manufacturing and development capabilities, are provided through its wholly-owned subsidiary Avid Bioservices, Inc. (www.avidbio.com), which provides development and biomanufacturing services for both Peregrine and third-party customers. The company is also working to evaluate its lead immunotherapy candidate, bavituximab, in combination with immune stimulating therapies for the treatment of various cancers, and developing its proprietary exosome technology for the detection and monitoring of cancer. For more information, please visit www.peregrineinc.com.
About Avid BioservicesAvid Bioservices provides a comprehensive range of process development, high quality cGMP clinical and commercial manufacturing services for the biotechnology and biopharmaceutical industries. With over 15 years of experience producing monoclonal antibodies and recombinant proteins in batch, fed-batch and perfusion modes, Avid's services include cGMP clinical and commercial product manufacturing, purification, bulk packaging, stability testing and regulatory strategy, submission and support. The company also provides a variety of process development activities, including cell line development and optimization, cell culture and feed optimization, analytical methods development and product characterization. For more information about Avid, please visit www.avidbio.com.
Safe Harbor Statement: Statements in this press release which are not purely historical, including statements regarding Peregrine Pharmaceuticals' intentions, hopes, beliefs, expectations, representations, projections, plans or predictions of the future are forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. The forward-looking statements involve risks and uncertainties including, but not limited to, the risk that a future clinical trial combining bavituximab with an immune checkpoint inhibitor my not generate statistically significant data, data consistent with the data presented at AACR regarding SUNRISE patients who were treated with bavituximab and subsequently treated with immune checkpoint inhibitors or data supporting the theory that bavituximab modulates the tumor microenvironment to complement and enhance anti-tumor activity of immune checkpoint inhibitors, the risk that one or more of the NCCN grant funded investigator-initiated clinical studies may experience enrollment delays, the risk that data from one or more of the NCCN grant funded investigator-initiated clinical studies does not support further evaluation, the risk that the results from the pre-clinical studies are not replicated in human clinical trials, the risk that the company may not have or raise adequate financial resources from debt and/or equity financings and/or Avid's manufacturing operations to enable it to continue as a going concern, or to fund the further development of bavituximab or further development of PS exosome diagnostic technology, the risk that data from further testing of the PS exosome diagnostic with human samples will not support further development, commercialization or contemplated partnering discussions, the risk that Avid's revenue growth may slow or decline, the risk that the company does not achieve profitability, the risk that Avid may experience technical difficulties in processing customer orders which could delay delivery of products to customers, revenue recognition and receipt of payment, the risk that one or more existing Avid customers terminates its contract prior to completion or reduces or delays its demand for manufacturing services, and the risk that commencement of construction of the new manufacturing facility will be delayed indefinitely due to a lack of customer demand and/or inability to raise the capital to construct the facility. The company's actual results could differ materially from those in any such forward-looking statements. Factors that could cause actual results to differ materially include, but are not limited to, uncertainties associated with completing preclinical and clinical trials for our technologies; the early stage of product development; the significant costs to develop our products as all of our products are currently in development, preclinical studies or clinical trials; obtaining additional financing to support our operations and the development of our products; obtaining regulatory approval for our technologies; anticipated timing of regulatory filings and the potential success in gaining regulatory approval and complying with governmental regulations applicable to our business. Our business could be affected by a number of other factors, including the risk factors listed from time to time in our reports filed with the Securities and Exchange Commission including, but not limited to, our annual report on Form 10-K for the fiscal year ended April 30, 2017 as well as any updates to these risk factors filed from time to time in the company's other filings with the Securities and Exchange Commission. The company cautions investors not to place undue reliance on the forward-looking statements contained in this press release. Peregrine Pharmaceuticals, Inc. disclaims any obligation, and does not undertake to update or revise any forward-looking statements in this press release.
PEREGRINE PHARMACEUTICALS, INC. | |||||||||||||||||
CONSOLIDATED STATEMENTS OF OPERATIONS AND COMPREHENSIVE LOSS | |||||||||||||||||
THREE MONTHS ENDEDAPRIL 30, | TWELVE MONTHS ENDEDAPRIL 30, | ||||||||||||||||
2017 | 2016 | 2017 | 2016 | ||||||||||||||
Unaudited | Unaudited | ||||||||||||||||
REVENUES: | |||||||||||||||||
Contract manufacturing revenue | $ | 17,904,000 | $ | 18,783,000 | $ | 57,630,000 | $ | 44,357,000 | |||||||||
License revenue | — | — | — | 329,000 | |||||||||||||
Total revenues | 17,904,000 | 18,783,000 | 57,630,000 | 44,686,000 | |||||||||||||
COSTS AND EXPENSES: | |||||||||||||||||
Cost of contract manufacturing | 11,782,000 | 9,721,000 | 38,259,000 | 22,966,000 | |||||||||||||
Research and development | 6,717,000 | 16,265,000 | 28,297,000 | 59,529,000 | |||||||||||||
Selling, general and administrative | 4,709,000 | 4,712,000 | 19,334,000 | 18,551,000 | |||||||||||||
Total costs and expenses | 23,208,000 | 30,698,000 | 85,890,000 | 101,046,000 | |||||||||||||
LOSS FROM OPERATIONS | (5,304,000 | ) | (11,915,000 | ) | (28,260,000 | ) | (56,360,000 | ) | |||||||||
OTHER INCOME (EXPENSE): | |||||||||||||||||
Interest and other income | 37,000 | 31,000 | 108,000 | 722,000 | |||||||||||||
Interest and other expense | (5,000 | ) | — | (7,000 | ) | (14,000 | ) | ||||||||||
NET LOSS | $ | (5,272,000 | ) | $ | (11,884,000 | ) | $ | (28,159,000 | ) | $ | (55,652,000 | ) | |||||
COMPREHENSIVE LOSS | $ | (5,272,000 | ) | $ | (11,884,000 | ) | $ | (28,159,000 | ) | $ | (55,652,000 | ) | |||||
Series E preferred stock accumulated dividends | (1,442,000 | ) | (1,380,000 | ) | (4,640,000 | ) | (4,484,000 | ) | |||||||||
NET LOSS ATTRIBUTABLE TO COMMON STOCKHOLDERS | $ | (6,714,000 | ) | $ | (13,264,000 | ) | $ | (32,799,000 | ) | $ | (60,136,000 | ) | |||||
WEIGHTED AVERAGE COMMON SHARES OUTSTANDING: | |||||||||||||||||
Basic and Diluted (1) | 42,141,720 | 33,478,863 | 37,109,493 | 30,895,089 | |||||||||||||
BASIC AND DILUTED LOSS PER COMMON SHARE (1) | $ | (0.16 | ) | $ | (0.40 | ) | $ | (0.88 | ) | $ | (1.95 | ) |
(1) All share and per share amounts of our common stock issued and outstanding for all periods have been retroactively adjusted to reflect the one-for-seven reverse stock split which took effect with the opening of trading on July 10, 2017.
PEREGRINE PHARMACEUTICALS, INC. | |||||||
CONSOLIDATED BALANCE SHEETS | |||||||
AS OF APRIL 30, 2017 AND 2016 | |||||||
2017 | 2016 | ||||||
ASSETS | |||||||
CURRENT ASSETS: | |||||||
Cash and cash equivalents | $ | 46,799,000 | $ | 61,412,000 | |||
Trade and other receivables | 7,742,000 | 2,859,000 | |||||
Inventories | 33,099,000 | 16,186,000 | |||||
Prepaid expenses | 1,460,000 | 1,351,000 | |||||
Total current assets | 89,100,000 | 81,808,000 | |||||
PROPERTY AND EQUIPMENT: | |||||||
Leasehold improvements | 20,098,000 | 19,610,000 | |||||
Laboratory equipment | 10,777,000 | 10,257,000 | |||||
Furniture, fixtures, office equipment and software | 4,499,000 | 4,045,000 | |||||
35,374,000 | 33,912,000 | ||||||
Less accumulated depreciation and amortization | (11,700,000 | ) | (9,610,000 | ) | |||
Property and equipment, net | 23,674,000 | 24,302,000 | |||||
Restricted cash | 1,150,000 | 600,000 | |||||
Other assets | 4,188,000 | 2,333,000 | |||||
TOTAL ASSETS | $ | 118,112,000 | $ | 109,043,000 |
PEREGRINE PHARMACEUTICALS, INC. | |||||||
CONSOLIDATED BALANCE SHEETS | |||||||
AS OF APRIL 30, 2017 AND 2016 (continued) | |||||||
2017 | 2016 | ||||||
LIABILITIES AND STOCKHOLDERS' EQUITY | |||||||
CURRENT LIABILITIES: | |||||||
Accounts payable | $ | 5,779,000 | $ | 8,429,000 | |||
Accrued clinical trial and related fees | 4,558,000 | 7,594,000 | |||||
Accrued payroll and related costs | 6,084,000 | 5,821,000 | |||||
Deferred revenue | 28,500,000 | 10,030,000 | |||||
Customer deposits | 17,017,000 | 24,212,000 | |||||
Other current liabilities | 993,000 | 1,488,000 | |||||
Total current liabilities | 62,931,000 | 57,574,000 | |||||
Deferred rent, less current portion | 1,599,000 | 1,395,000 | |||||
Commitments and contingencies | |||||||
STOCKHOLDERS' EQUITY (1): | |||||||
Preferred stock - $.001 par value; authorized 5,000,000 shares;issued and outstanding - 1,647,760 and 1,577,440, respectively | 2,000 | 2,000 | |||||
Common stock - $.001 par value; authorized 500,000,000shares; issued and outstanding - 44,014,040 and 33,847,213,respectively | 44,000 | 34,000 | |||||
Additional paid-in-capital | 590,971,000 | 559,314,000 | |||||
Accumulated deficit | (537,435,000 | ) | (509,276,000 | ) | |||
Total stockholders' equity | 53,582,000 | 50,074,000 | |||||
TOTAL LIABILITIES AND STOCKHOLDERS' EQUITY | $ | 118,112,000 | $ | 109,043,000 | |||
(1) All share and per share amounts of our common stock issued and outstanding for all periods have been retroactively adjusted to reflect the one-for-seven reverse stock split which took effect with the opening of trading on July 10, 2017.
The photo is also available at Newscom, www.newscom.com, and via AP PhotoExpress.
Contacts: Stephanie Diaz (Investors) Vida Strategic Partners 415-675-7401 sdiaz@vidasp.com Tim Brons (Media) Vida Strategic Partners 415-675-7402 tbrons@vidasp.com
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