Agenus R&D Update & Third Quarter Financial Report
Agenus Inc. (NASDAQ: AGEN) provided a corporate update alongside its Q3 2020 financial results. The company initiated its rolling BLA filing for Balstilimab, with FDA review in progress. Recent clinical trials show Balstilimab achieving a 19% response rate in PD-L1 positive tumors and a combination with zalifrelimab yielding 27%. The cash balance rose to $114 million, while Q3 net loss was $52 million, a slight increase from $46 million in Q3 2019. Revenues totaled $14.8 million, down from $19.9 million in the prior year. New data on AGEN1181 will be presented at the upcoming SITC meeting.
- Initiated rolling BLA filing for Balstilimab, FDA review ongoing.
- Balstilimab shows promising response rates: 19% in PD-L1 positive tumors.
- Combination trial of Balstilimab and zalifrelimab achieves a 27% response rate.
- Increased cash balance to $114 million from $62 million at end of 2019.
- Q3 net loss increased to $52 million compared to $46 million in Q3 2019.
- Total revenues decreased to $14.8 million from $19.9 million year-over-year.
- Cash used in operations increased to $32 million from $28 million in the same quarter of 2019.
- Balstilimab rolling BLA filing and FDA review underway
- COVID-19 trial open with patients in screening for iNKT Cell Therapy
- New data and clinical responses with AGEN1181 to be presented at SITC on NOV11
LEXINGTON, Mass., Oct. 29, 2020 (GLOBE NEWSWIRE) -- Agenus Inc. (NASDAQ: AGEN), an immuno-oncology company with an extensive pipeline of checkpoint antibodies, cell therapies, adjuvants, and vaccines designed to activate and optimize immune response to cancers and infections, today provided a corporate update and reported financial results for the third quarter of 2020.
- Balstilimab BLA filing initiated and FDA review is underway; data presented at ESMO
- Balstilimab (PD-1) monotherapy trial achieves response rates of
19% in PD-L1 positive tumors and14% in PD-L1 positive and negative tumors combined - Balstilimab (PD-1) + zalifrelimab (CTLA-4) combination trial achieves response rates of
27% in PD-L1 positive tumors and22% in PD-L1 positive and negative tumors combined - Median duration of response of 15.4 months demonstrated for monotherapy; median duration of response in the combination trial has not yet been reached
- Balstilimab (PD-1) monotherapy trial achieves response rates of
- Allogeneic iNKT cell therapy: patients with COVID-19 in screening
- iNKT cells have unique properties to combat cancer and infections
- iNKT cells regulate harmful inflammation while also preventing reinfection
- iNKT cancer clinical trial expected to commence in 4Q2020
- Seven AGEN programs to be presented at SITC
- AGEN1181: new data and responses of AGEN1181 alone and with balstilimab
- Zalifrelimab: clinical activity in refractory rare tumors
- Balstilimab +/- zalifrelimab: improving treatment of cervical cancer patients with pseudo-progression
- AGEN2373: anti-CD137 antibody designed for optimal safely and efficacy
- AGEN1777: Fc-enhanced TIGIT bispecific for optimal anti-tumor action
- iNKT cell therapy: cancer killing with unmodified iNKTs as well as CAR-iNKTs
- AGEN VISION platform: identification of biomarkers and new targets, prediction of responders
- Partnered program MK-4830 presented at ESMO
- MK-4830 (ILT4 agonist licensed to Merck) shows benefit as a monotherapy and in combo with anti-PD-1 with 11 responses (2CR, 9PRs)
- Agenus already received
$10M in milestones and is eligible to receive an additional$85M
- Launch of balstilimab access program with Rottapharm
- Agenus provides balstilimab to Rottapharm for clinical testing with CR6086, a potent and selective prostaglandin EP4 receptor antagonist, in patients with advanced metastatic colorectal cancer; trial expected to commence by end of 2020
- Agenus provides balstilimab to Rottapharm for clinical testing with CR6086, a potent and selective prostaglandin EP4 receptor antagonist, in patients with advanced metastatic colorectal cancer; trial expected to commence by end of 2020
Third Quarter Financial Results
We ended the third quarter of 2020 with a cash balance of
For the third quarter ended September 30, 2020, our cash used in operations was
Our cash used in operations for the nine months ended September 30, 2020 was
For the nine-month period ended September 30, 2020, we recognized revenue of
| Financial Highlights | ||||||||||||||||
| (in thousands, except per share data) | ||||||||||||||||
| (unaudited) | ||||||||||||||||
| September 30, 2020 | December 31, 2019 | |||||||||||||||
| Cash and cash equivalents | $ | 114,144 | $ | 61,808 | ||||||||||||
| Three months ended September 30, | Nine months ended September 30, | |||||||||||||||
| 2020 | 2019 | 2020 | 2019 | |||||||||||||
| Revenues, research and development | $ | 4,287 | $ | 5,751 | $ | 24,284 | $ | 81,022 | ||||||||
| Revenues, non-cash royalty | 8,947 | 12,204 | 29,950 | 30,073 | ||||||||||||
| Revenues, other | 1,599 | 1,985 | 2,672 | 4,453 | ||||||||||||
| Total Revenue | 14,833 | 19,940 | 56,906 | 115,548 | ||||||||||||
| Research and development expenses | 32,134 | 46,132 | 107,047 | 131,506 | ||||||||||||
| General and administrative expenses | 14,380 | 11,512 | 39,188 | 33,723 | ||||||||||||
| Cost of service revenue | 911 | - | 1,545 | - | ||||||||||||
| Other expense (income) | 940 | (437 | ) | 2,806 | (552 | ) | ||||||||||
| Non-cash interest expense | 15,918 | 10,791 | 44,109 | 30,400 | ||||||||||||
| Loss on modification of debt | - | - | 2,720 | - | ||||||||||||
| Non-cash contingent consideration fair value adjustment | 2,196 | (1,781 | ) | 4,652 | 1,180 | |||||||||||
| Net loss | $ | (51,646 | ) | $ | (46,277 | ) | $ | (145,161 | ) | $ | (80,709 | ) | ||||
| Net loss per share attributable to Agenus Inc. common stockholders | $ | (0.28 | ) | $ | (0.33 | ) | $ | (0.87 | ) | $ | (0.58 | ) | ||||
| Cash (used in) provided by operations | $ | (31,626 | ) | $ | (27,785 | ) | $ | (103,506 | ) | $ | 13,098 | |||||
Call Access
To access the live call, dial (833) 614-1394 (US) or (914) 987-7115 (International)
The call will also be webcast and will be accessible from the Company website’s Events & Presentations page at https://investor.agenusbio.com/events-and-presentations or via https://edge.media-server.com/mmc/p/mbkjgw8w. A replay will be available after the call.
About Agenus
Agenus is a clinical-stage immuno-oncology company focused on the discovery and development of therapies that engage the body's immune system to fight cancer. The Company's vision is to expand the patient populations benefiting from cancer immunotherapy by pursuing combination approaches that leverage a broad repertoire of antibody therapeutics, adoptive cell therapies (through its AgenTus Therapeutics subsidiary), and proprietary cancer vaccine platforms. The Company is equipped with a suite of antibody discovery platforms and a state-of-the-art GMP manufacturing facility with the capacity to support clinical programs. Agenus is headquartered in Lexington, MA. For more information, please visit www.agenusbio.com and our Twitter handle @agenus_bio. Information that may be important to investors will be routinely posted on our website and Twitter.
Forward-Looking Statements
This press release contains forward-looking statements that are made pursuant to the safe harbor provisions of the federal securities laws, including statements regarding clinical development and regulatory plans and timelines, anticipated corporate milestones, new clinical data and program updates to be presented at SITC and the anticipated commencement of Agenus’ clinical collaboration with Rottapharm. These forward-looking statements are subject to risks and uncertainties that could cause actual results to differ materially. These risks and uncertainties include, among others, the factors described under the Risk Factors section of our most recent Quarterly Report on Form 10-Q or Annual Report on Form 10-K filed with the Securities and Exchange Commission. Agenus cautions investors not to place considerable reliance on the forward-looking statements contained in this release. These statements speak only as of the date of this press release, and Agenus undertakes no obligation to update or revise the statements, other than to the extent required by law. All forward-looking statements are expressly qualified in their entirety by this cautionary statement.
Contact
Agenus Inc.
Caroline Bafundo
212-994-8209
Caroline.bafundo@agenusbio.com
FAQ
What were Agenus's Q3 2020 revenue figures?
How did Agenus perform financially in Q3 2020 compared to Q3 2019?
What is the status of Balstilimab's FDA approval?
What new data on AGEN1181 will be presented, and when?
