Grab Sources And More Here: Company Website. Company Presentation. -----
As mentioned above, (NYSE American: MAIA) has several explosive potential catalysts to consider right now. Check these out:
#1. MAIA Potential Catalyst - One Analyst's Target Suggests Over 600% Potential Upside From MAIA's Current Chart Levels.
Last month, Robert LeBoyer, Senior Vice President and equity research analyst with Noble Life Science Partners, reiterated a $14.00 target on MAIA.
From Tuesday's closing valuation, that provides MAIA with upside potential well over 600%!
Check out some key report highlights:
Conclusion. Roche becomes the third pharmaceutical company to make a supply agreement with MAIA to test a checkpoint inhibitor in combination with THIO. We believe this shows that potential partners have noticed the data showing improved overall survival (OS), progression free survival (PFS), and the side effect profile. Clinical data from the three of the eight approved checkpoint inhibitors could make bidding for a marketing partnership more competitive. We are reiterating our Outperform rating and $14 price target. -----
#2. MAIA Potential Catalyst - Volatility Could Be In Full Force Based On MAIA's Low Float.
According to info from the Yahoo Finance website, MAIA has a relatively low float.
The website reports this profile to have roughly 25.65Mn shares in its float.
Why is that important? It's important on one crucial level. Volatility potential.
Could even more positive company news in mid-2025 provide a breakout spark? -----
#3. MAIA Potential Catalyst - MAIA Biotechnology Announced A New PR As Patient's Tumor Size Decreases By At Least 30%.
MAIA Biotechnology Announces New Responder in Non-Small Cell Lung Cancer Phase 2 Clinical Trial
CHICAGO, June 05, 2025--(BUSINESS WIRE)--MAIA Biotechnology, Inc. (NYSE American: MAIA) ("MAIA", the "Company"), a clinical-stage biopharmaceutical company focused on developing targeted immunotherapies for cancer, today announced a new partial response (PR) was identified in a patient after 20 months of treatment in its Phase 2 THIO-101 clinical trial evaluating ateganosine (THIO), sequenced with Regeneron’s immune checkpoint inhibitor (CPI) cemiplimab (Libtayo®) in patients with advanced non-small cell lung cancer (NSCLC) who are resistant to immune therapy and chemotherapy. A partial response is defined as a decrease in tumor size of at least 30%.
"The patient remained on treatment and we observed stable disease for more than twenty months before the partial response was identified, highlighting the efficacy, safety and low toxicity of the treatment. Extended-term responses like this are not often seen in heavily pretreated patients in hard-to-treat diseases such as NSCLC, where the prognosis for the advanced-stage of the disease is typically poor," said MAIA Chairman and CEO Vlad Vitoc, M.D. "We confirmed this response with a second scan, and we are highly confident that ateganosine could become an outstanding therapeutic alternative for third-line NSCLC patients."
THIO-101 third line (3L) data cutoff from May 15, 2025, showed median overall survival (OS) of 17.8 months for the 22 NSCLC patients who received at least one dose of ateganosine in parts A and B of the trial. At the data cutoff, the patient with the longest survival in the trial had completed 32 cycles of therapy and had 24.3 months survival. Studies of standard-of-care (SOC) chemotherapy treatments for NSCLC in a similar setting have shown OS of 5 to 6 months.1
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Read the full article here. -----
#4. MAIA Potential Catalyst - MAIA Biotechnology Enters Into A Key Supply Agreement With Roche For Future Studies.
MAIA Biotechnology Announces Master Clinical Supply Agreement with Roche for Hard-to-Treat Cancer Therapies
Agreement to support future studies investigating the combination of ateganosine and atezolizumab for safe and effective cancer treatments
CHICAGO, June 18, 2025--(BUSINESS WIRE)--MAIA Biotechnology, Inc. (NYSE American: MAIA), a clinical-stage biopharmaceutical company focused on developing targeted immunotherapies for cancer, today announced its entry into a clinical master supply agreement with Roche for future studies investigating the combination of MAIA’s telomere-targeting agent ateganosine (THIO), sequenced with Roche’s checkpoint inhibitor (CPI), atezolizumab (Tecentriq®), for the treatment of multiple hard-to-treat cancers.
"In preclinical studies, ateganosine was found to be highly synergistic and effective in combination with Roche’s anti-PD-L1 agent atezolizumab," said MAIA Chairman and CEO Vlad Vitoc, M.D. "We are pleased to partner with world-renowned Roche and we look forward to further strengthening our mission to find safe and effective cancer treatments."
Read the full article here. -----
#5. MAIA Potential Catalyst - MAIA Welcomes Experts To Board, Strengthening Oncology Innovation Leadership Team.
MAIA Biotechnology Welcomes Leading Hepatocellular Carcinoma Clinician-Scientists to Scientific Advisory Board
Planning for Phase 2 clinical trial in hepatocellular carcinoma (HCC) underway
CHICAGO, June 24, 2025--(BUSINESS WIRE)--MAIA Biotechnology, Inc. (NYSE American: MAIA) ("MAIA", the "Company"), a clinical-stage biopharmaceutical company focused on developing targeted immunotherapies for cancer, today announced the appointment of two prominent oncologists to its Scientific Advisory Board (SAB), Claudia Fulgenzi, MD, and David J. Pinato, MD, MRCP (UK), PhD. Both are specialists in hepatocellular carcinoma (HCC), a tumor type to be studied in future clinical trials of MAIA’s lead candidate ateganosine (THIO) sequenced with a checkpoint inhibitor.
As SAB members they will advise MAIA on designs and protocols for its company sponsored trial (CST) in HCC and may participate in future investigator sponsored trials (IST).
"Drs. Pinato and Fulgenzi are scientific experts on inflammation as a pathogenic and prognostic mechanism in primary liver cancers. Together, their research has focused on improving the treatment of HCC, particularly with the use of anti-cancer immunotherapy," said MAIA Chairman and CEO Vlad Vitoc, M.D. "They will bring a wealth of knowledge to our SAB, with specialized expertise that will inform our plans and preparations for our upcoming clinical program in HCC."
"By the end of this year, we expect to have all required approvals to begin enrolling patients in a HCC trial," Dr. Vitoc added.
...
Read the full article here. -----
MAIA Recap - This NYSE American Breakout Idea Has 5 Explosive Potential Catalysts
#1. One Analyst's Target Suggests Over 600% Potential Upside From MAIA's Current Chart Levels.
#2. Volatility Could Be In Full Force Based On MAIA's Low Float.
#3. MAIA Biotechnology Announced A New PR As Patient's Tumor Size Decreases By At Least 30%.
#4. MAIA Biotechnology Enters Into A Key Supply Agreement With Roche For Future Studies.
#5. MAIA Welcomes Experts To Board, Strengthening Oncology Innovation Leadership Team. -----
Coverage is officially reinitiated on (NYSE American: MAIA). When updates are available, I'll get them out quickly. Talk soon.
Sincerely, Kai Parker StockWireNews
(Always Remember The St-ock Prices Could Be Significantly Lower Now From The Dates I Provided.) |
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