Full Press Release Details
Reports Second Quarter 2016 Financial Results and Operational Progress
to host conference call at 11:00 a.m. ET today
LEXINGTON, Mass.--(BUSINESS WIRE)--July 28, 2016--Agenus Inc. (NASDAQ:
AGEN), an immuno-oncology (I-O) company developing antibodies, including
checkpoint inhibitors and other checkpoint modulators, and cancer
vaccines, today provided a corporate update and reported financial
results for the second quarter ended June 30, 2016.
"In the second quarter, we made important advances in the clinic, saw
external validation of our immuno-oncology agents and strategy and
further integrated our capabilities to improve speed, cost and quality
of product development efforts," said Garo H. Armen, Ph.D., Chairman and
CEO of Agenus. "We also strengthened our management team with the
addition of a new Board member, Ulf Wiinberg, and Global Head of
Clinical Development, Dr. Jean-Marie Cuillerot."
Second Quarter 2016 and Recent Corporate Highlights
July: Completed enrollment of the first cohort of patients in the
Phase 1 study of AGEN1884, an anti-CTLA-4 antibody, which was launched
earlier in 2016. Agenus plans to initiate clinical studies for
a second anti-CTLA-4 antibody, AGEN2041, in 2017 and start combination
trials with AGEN1884 in the first half of 2017.
July: Appointed Jean-Marie Cuillerot, M.D. as Vice President and
Global Head of Clinical Development, bringing extensive
immuno-oncology clinical development expertise to the Company's I-O
portfolio. In Dr. Cuillerot's previous role at a Merck Serono
affiliate, he advanced the PD-L1 antibody avelumab from pre-IND to
regulatory filing and delivered the dataset leading to the $880
million co-development deal with Pfizer. At Bristol-Myers Squibb, he
developed clinical strategies for the anti-CTLA-4 antibody ipilimumab
as a treatment for lung cancer, castrate resistant prostate cancer,
ovarian cancer, gastric cancer and glioblastoma, and supported the
filing activities of ipilimumab for first-line treatment of melanoma.
June: Initiated Phase 1/2 clinical trial of anti-GITR
checkpoint antibody INCAGN1876 in solid tumors in
collaboration with Incyte. INCAGN1876 is the second product candidate
from the Company's antibody program to advance into clinical trials
June: Merck selected a lead product candidate to advance
into preclinical studies under our research collaboration, leading
to receipt of a $2 million milestone payment. The achievement
further validates Agenus' discovery platform, which is capable of
identifying unique antibodies for a broad range of therapeutic
targets. Under the terms of the agreement, Merck will be responsible
for all future product development expenses for the selected antibody
candidate targeting an undisclosed Merck checkpoint target. Agenus is
eligible to receive up to $100 million in milestone payments, in
addition to royalties on worldwide product sales.
May: Appointed Ulf Wiinberg to the Company's Board of
Directors. Ulf brings over 30 years of experience in the
pharmaceutical industry with senior leadership roles at multiple
global drug development companies. Most recently, he served as Chief
Executive Officer of H. Lundbeck A/S, and previously held multiple
executive roles at Wyeth, one of the world's largest research-driven
pharmaceutical companies. Currently, he serves on the boards of
multiple drug companies including Avillion, Hansa Medical, Nestle
Health Sciences and UCB SA.
Second Quarter 2016 Financial Results
For the second quarter ended June 30, 2016, Agenus reported a net loss
attributable to common stockholders of $28.4 million which includes $7.6
million of non-cash expenses. This compares to a net loss attributable
to common stockholders for the second quarter of 2015 of $40.5 million
which included $17.3 million of non-cash expenses. Net loss was $0.33
per share, and $0.53 per share, basic and diluted, for the three months
ended June 30, 2016 and 2015, respectively. The decrease in net loss
attributable to common stockholders for the three months ended June 30,
2016, compared to the net loss attributable to common stockholders for
the same period in 2015, was primarily due to the $13.2 million charge
for the purchase of the SECANT yeast display platform in 2015 and the
non-cash expense from fair value adjustments of the contingent
obligations partially offset by the advancement of the checkpoint
For the six months ended June 30, 2016, the company reported a net loss
attributable to common stockholders of $60.2 million, which includes
$17.2 million in non-cash expenses, compared with a net loss
attributable to common stockholders of $59.3 million, which included
$26.5 million in non-cash expenses, for the six months ended June 30,
2015. Net loss was $0.69 per share and $0.83 per share, basic and
diluted for the six months ended June 30, 2016 and 2015, respectively.
Cash, cash equivalents and short-term investments were $123.3 million as
Conference Call, Webcast and Prepared Statement Information
Agenus executives will host a conference call at 11:00 a.m. ET today. To
access the live call, dial 1-888-799-5016 (U.S.) or 1-704-908-0465
(international) and refer to conference ID number 50188771. The call
will also be webcast and will be accessible from the Company's website
at www.agenusbio.com/webcast. A replay will be available on the
Company's website approximately two hours after the call and will remain
available for 60 days.
Agenus is an immuno-oncology company focused on the discovery and
development of revolutionary new treatments that engage the body's
immune system to benefit patients suffering from cancer. By combining
multiple powerful platforms, Agenus has established a highly integrated
approach for the discovery, development and manufacture of monoclonal
antibodies that modulate targets of interest. In addition, the Company's
cancer vaccine program includes three proprietary platforms focused on
individualized and off-the-shelf vaccines uniquely designed for each
patient. Agenus' broad portfolio of novel checkpoint and other
immuno-modulatory monoclonal antibodies, vaccines and adjuvants work in
combination to provide the opportunity to create best-in-class
therapeutic regimens. The Company has formed collaborations with Merck
and Incyte to discover and develop multiple checkpoint antibodies. For
more information, please visit www.agenusbio.com; information
that may be important to investors will be routinely posted on our
| Condensed Consolidated Statements of Operations Data | |||||||||||||||||||
| (in thousands, except per share data) | |||||||||||||||||||
| (unaudited) | |||||||||||||||||||
| Three months ended June 30, | Six months ended June 30, | ||||||||||||||||||
| 2016 | 2015 | 2016 | 2015 | ||||||||||||||||
| Revenue | $ | 6,592 | $ | 6,377 | $ | 12,551 | $ | 10,330 | |||||||||||
| Operating expenses: | |||||||||||||||||||
| Research and development | 22,362 | 24,773 | 47,400 | 33,993 | |||||||||||||||
| General and administrative | 7,117 | 8,016 | 16,349 | 13,503 | |||||||||||||||
| Non-cash contingent consideration fair value adjustment | 721 | 6,783 | 379 | 14,321 | |||||||||||||||
| Operating loss | (23,608 | ) | (33,195 | ) | (51,577 | ) | (51,487 | ) | |||||||||||
| Other expense, net | (4,712 | ) | (7,215 | ) | (8,521 | ) | (7,665 | ) | |||||||||||
| Net loss | (28,320 | ) | (40,410 | ) | (60,098 | ) | (59,152 | ) | |||||||||||
| Dividends on Series A-1 convertible preferred stock | (51 | ) | (51 | ) | (102 | ) | (101 | ) | |||||||||||
| Net loss attributable to common stockholders | $ | (28,371 | ) | $ | (40,461 | ) | $ | (60,200 | ) | $ | (59,253 | ) | |||||||
| Per common share data, basic and diluted: | |||||||||||||||||||
| Net loss attributable to common stockholders | $ | (0.33 | ) | $ | (0.53 | ) | $ | (0.69 | ) | $ | (0.83 | ) | |||||||
| Weighted average number of common shares outstanding, basic and diluted | 86,965 | 76,375 | 86,826 | 71,548 |