Please wait while we load the requested 10-K report or click the link below:
https://last10k.com/sec-filings/report/1724521/000156459019006274/rcus-10k_20181231.htm
March 2023
February 2023
December 2022
November 2022
November 2022
October 2022
August 2022
June 2022
May 2022
February 2022
Exhibit 99.1
Arcus Biosciences Announces Fourth Quarter and Full Year 2018 Financial Results and Recent Corporate Updates
|
- |
Ended 2018 with four molecules in clinical development, including AB928, the Company’s dual A2aR/A2bR receptor antagonist, which is being evaluated in several dose-escalation trials in combination with chemotherapy or AB122 (anti-PD-1 antibody) |
|
- |
Also ongoing are a Phase 1 trial of AB154 (anti-TIGIT antibody) in patients with advanced solid tumors, alone and in combination with AB122, as well as a trial of AB680 (CD73 inhibitor) in healthy volunteers |
|
- |
Ended 2018 with $259.7 million in cash and investments |
Hayward, CA. – (BUSINESS WIRE) – March 5, 2019 -
Arcus Biosciences, Inc. (NYSE:RCUS), a clinical-stage biopharmaceutical company focused on creating innovative cancer immunotherapies, today announced financial results for the fourth quarter and full year 2018. The Company also provided updates on its clinical programs.
“Throughout 2018, we made substantial progress on multiple programs, ending the year with four product candidates in the clinic,” said Terry Rosen, Ph.D., Chief Executive Officer at Arcus. “Enrollment continues in our first three dose-escalation trials for AB928, in which we are evaluating AB928 in combination with either immunogenic chemotherapies or our anti-PD-1 antibody, AB122, across a number of tumor types. We plan to present early data on safety, pharmacokinetic/pharmacodynamic profile, biomarker analysis and clinical activity for the AB928 combinations in mid-2019. Following our IPO last year, we have a strong balance sheet, and we are well-positioned to execute on our research and clinical development plans into 2021.”
Pipeline Updates
AB928 (dual A2aR/A2bR antagonist)
|
• |
AB928 in combination with Doxil® in triple negative breast cancer (TNBC) and ovarian cancer |
|
• |
AB928 in combination with mFOLFOX in colorectal cancer and gastroesophageal cancer |
|
• |
AB928 in combination with AB122 in advanced solid tumors. |
• |
The Company expects to initiate its fourth AB928 combination trial in patients in the coming months: |
|
• |
AB928 in combination with carboplatin/pemetrexed with or without pembrolizumab in non-small cell lung cancer (NSCLC) after failing tyrosine kinase inhibitor (TKI) therapy. |
• |
The Company is enrolling the final cohort of the Phase 1 dose-escalation trial for AB122. Based on data generated to date, the Company selected 240 mg as the dose for the Q2W (every 2 weeks) |
Please wait while we load the requested 10-K report or click the link below:
https://last10k.com/sec-filings/report/1724521/000156459019006274/rcus-10k_20181231.htm
Compare this 10-K Annual Report to its predecessor by reading our highlights to see what text and tables were removed , added and changed by Arcus Biosciences, Inc..
Arcus Biosciences, Inc.'s Definitive Proxy Statement (Form DEF 14A) filed after their 2019 10-K Annual Report includes:
Financial Statements, Disclosures and Schedules
Inside this 10-K Annual Report
Material Contracts, Statements, Certifications & more
Arcus Biosciences, Inc. provided additional information to their SEC Filing as exhibits
Ticker: RCUS
CIK: 1724521
Form Type: 10-K Annual Report
Accession Number: 0001564590-19-006274
Submitted to the SEC: Tue Mar 05 2019 4:16:30 PM EST
Accepted by the SEC: Tue Mar 05 2019
Period: Monday, December 31, 2018
Industry: Pharmaceutical Preparations