Antibe Therapeutics Reports Q1 2023 Interim Financial and Operating Results
Antibe Therapeutics Inc. (OTCQX: ATBPF) announced its financial results for the quarter ended June 30, 2022. The company reported a net loss of $5.5 million but retains a strong cash position of $50 million, providing over two years of operational runway. Antibe is set to initiate a Phase II trial for its lead drug, otenaproxesul, targeting acute pain in September 2022. Additionally, the company is advancing its inflammatory bowel disease program and has signed an agreement to sell Citagenix for $6.5 million. Upcoming milestones include trial results expected early in 2023.
- Cash position of $50 million ensures over two years of operational runway.
- Progress in Phase II acute pain program with trial initiation in September 2022.
- Identified three promising candidates for inflammatory bowel disease program.
- Agreement to sell Citagenix for $6.5 million bolsters financial resources.
- Net loss for the quarter increased slightly to $5.5 million from $6.3 million.
- Phase II acute pain program to initiate in September
- Ended quarter with
“We are really pleased with our progress,” commented
Business Highlights and Operational Update
Preparations on track for otenaproxesul’s Phase II program for acute pain
- Completed loading dose pharmacokinetic/pharmacodynamic (“PK/PD”) study in the quarter; results suggest viable onset of action for acute pain relief
-
Upcoming Phase II molar (wisdom tooth) extraction study to obtain PK/PD data and exploratory pain endpoints in post-operative patients – study to initiate in September with results expected by
January 2023 - Ongoing investigation of alternative treatment regimens as a potential path forward for chronic indications
Inflammatory bowel disease program nearing lead selection
- Identified three additional promising candidates for inflammatory bowel disease program – lead candidate to be chosen next quarter
Corporate and governance
-
Signed binding agreement to sell
Citagenix in a all-cash transaction, including milestones$6.5 million -
Appointed
Robert E. Hoffman as new Board Chair; former Chair,Walt Macnee , and Antibe’s founder, Dr.John L. Wallace , appointed as corporate Vice Chairs
Upcoming Milestones
The following summarizes the Company’s estimated timeline for its key upcoming milestones:
- Phase II third molar extraction trial initiation – calendar Q3 2022
- Identify lead candidate for inflammatory bowel disease – calendar Q4 2022
- Phase II third molar extraction trial results – early calendar Q1 2023
- Phase II bunionectomy trial initiation – calendar H1 2023
Financial Results
Cash Position: As of
Net Loss: For the quarter ended
Research and Development Expenses: Research and development expenses for the quarter, net of research tax credits, amounted to
General and Administrative Expenses: General and administrative expenses were
The Company’s unaudited fiscal Q1 2023 condensed interim financial statements and MD&A will be available shortly on SEDAR.
About
Antibe is a clinical stage biotechnology company leveraging its proprietary hydrogen sulfide platform to develop next-generation safer therapies to target inflammation arising from a wide range of medical conditions. The Company’s current pipeline includes assets that seek to overcome the gastrointestinal (“GI”) ulcers and bleeding associated with nonsteroidal anti-inflammatory drugs (“NSAIDs”). Antibe’s lead drug, otenaproxesul, is in clinical development as a safer alternative to opioids and today’s NSAIDs for acute pain. Antibe’s second pipeline drug, ATB-352, is being developed for a specialized pain indication. The Company’s anticipated next target is inflammatory bowel disease (“IBD”), a condition long in need of safer, more effective therapies. Learn more at antibethera.com.
Forward Looking Information
This news release includes certain forward-looking statements under applicable securities laws, which may include, but are not limited to, the anticipated scope, timing, duration and completion of certain of the Company’s clinical trial programs and studies and the anticipated timing for seeking market approval for certain of the Company’s drugs and therapies for certain additional indications. Any statements contained herein that are not statements of historical facts may be deemed to be forward-looking, including those identified by the expressions “will”, “anticipate”, “believe”, “plan”, “estimate”, “expect”, “intend”, “propose” and similar wording. Forward-looking statements involve known and unknown risks and uncertainties that could cause actual results, performance, or achievements to differ materially from those expressed or implied in this news release. Factors that could cause actual results to differ materially from those anticipated in this news release include, but are not limited to, the Company’s inability to timely execute on its business strategy and timely and successfully compete its clinical trials and studies, the Company’s inability to obtain the necessary regulatory approvals related to its activities, risks associated with drug and medical device development generally and those risk factors set forth in the Company’s public filings made in
View source version on businesswire.com: https://www.businesswire.com/news/home/20220815005193/en/
VP Investor Relations
+1 416-577-1443
christina@antibethera.com
Source:
FAQ
What are the key financial results for Antibe Therapeutics for the quarter ended June 30, 2022?
What is the status of Antibe's Phase II acute pain program?
When can we expect results from Antibe's third molar extraction trial?
How much is Antibe Therapeutics selling Citagenix for?