Antibe Therapeutics Reports Q3 2022 Interim Financial and Operating Results
Antibe Therapeutics Inc. has initiated its acute pain clinical program for otenaproxesul and ended the quarter with a
- Initiated acute pain clinical program for otenaproxesul.
- Cash position improved to
$59 million . - Net loss decreased to
$4.8 million compared to$6.5 million the previous year. - Filed new patent applications, potentially extending IP protection into the 2040s.
- Advanced multiple programs including those targeting inflammatory bowel disease.
- Available cash decreased from
$72 million as ofMarch 31, 2021 . - Ongoing net losses indicate continued financial strain.
- Acute pain clinical program for otenaproxesul initiating this quarter
- Ended quarter with a
“We’re excited to have launched otenaproxesul’s clinical program for post-operative pain and remain on track to begin Phase II in the fall. We’re also encouraged by draft guidance published last week by both the FDA and
Business Highlights
Launching otenaproxesul’s clinical program for post-operative pain
- First human pharmacokinetic/pharmacodynamic (“PK/PD”) study underway to determine optimal treatment regimens
- Preliminary third-party commercial assessment completed, confirming attractive market potential; comprehensive market opportunity and reimbursement study initiated
- Ongoing investigation of alternative treatment regimens as a potential path forward for chronic indications
Other pipeline drugs advancing
- Launched preclinical studies for specialized pain indication for ATB-352
- Identified several inflammatory bowel disease (“IBD”) candidates with encouraging preliminary results; animal proof-of-concept studies underway to select lead candidate
Bolstering intellectual property (“IP”) position
- Filed new patent application covering uses of otenaproxesul for treatment of acute pain; potential for IP protection to extend into the 2040s
- Filed trademark applications in all major markets for two proprietary brand names
Upcoming Milestones
The following summarizes the Company’s estimated timeline for its key upcoming milestones (calendar quarters):
- Initiate otenaproxesul PK/PD clinical studies – Q1 2022 (underway)
- Complete comprehensive market opportunity and reimbursement study – Q2 2022
- Identify lead IBD candidate– Q3 2022
- Determine optimal treatment regimens for otenaproxesul – Q3 2022
- Initiate otenaproxesul Phase II bunionectomy trial – Q4 2022
Financial Results
Cash Position: As of
Net Loss: For the quarter ended
Research and Development Expenses: Research and development expenses, net of research tax credits, amounted to
General and Administrative Expenses: General and administrative expenses totaled
The Company's unaudited fiscal Q3 2022 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 post-operative 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/20220214005249/en/
VP Investor Relations
+1 416-577-1443
christina@antibethera.com
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