MAIA Biotechnology enters clinical supply agreement with BeiGene for THIO
Written by Emily J. Thompson, Senior Investment Analyst
Updated: Jan 07 2025
0mins
Clinical Supply Agreement: MAIA Biotechnology has partnered with BeiGene to conduct Phase 2 trials assessing the efficacy of its anticancer agent THIO in combination with BeiGene's immune checkpoint inhibitor, tislelizumab, across three cancer types: hepatocellular carcinoma, small cell lung cancer, and colorectal cancer.
Preclinical Success and Future Plans: Preclinical studies have shown promising results for THIO, converting non-responsive tumors into responsive ones, and MAIA aims for accelerated FDA approvals while retaining global rights to develop THIO with other agents.
Trade with 70% Backtested Accuracy
Stop guessing "Should I Buy MAIA?" and start using high-conviction signals backed by rigorous historical data.
Sign up today to access powerful investing tools and make smarter, data-driven decisions.
Analyst Views on MAIA
Wall Street analysts forecast MAIA stock price to rise
1 Analyst Rating
1 Buy
0 Hold
0 Sell
Moderate Buy
Current: 1.270
Low
14.00
Averages
14.00
High
14.00
Current: 1.270
Low
14.00
Averages
14.00
High
14.00
No data
About MAIA
MAIA Biotechnology, Inc. is a clinical-stage biopharmaceutical company developing targeted immunotherapies for cancer. The Company's THIO (6-thio-dG, 6-thio-2'-deoxyguanosine), is a lead asset, is an investigational dual mechanism of action drug candidate incorporating telomere targeting and immunogenicity. The modified nucleotide 6-thio-2-deoxyguanosine (THIO) induces telomerase-dependent telomeric DNA modification, DNA damage responses, and selective cancer cell death. THIO-damaged telomeric fragments accumulate in cytosolic micronuclei and activates both innate (cGAS/STING) and adaptive (T-cell) immune responses. The sequential treatment with THIO followed by PD-(L)1 inhibitors resulted in tumor regression in advanced, in vivo cancer models by induction of cancer type-specific immune memory. THIO is being developed as a second or later line of treatment for NSCLC for patients that have progressed beyond the standard-of-care regimen of existing checkpoint inhibitors.
About the author
Emily J. Thompson
Emily J. Thompson, a Chartered Financial Analyst (CFA) with 12 years in investment research, graduated with honors from the Wharton School. Specializing in industrial and technology stocks, she provides in-depth analysis for Intellectia’s earnings and market brief reports.
MAIA Biotechnology Expands Phase 2 Trial for Ateganosine
- Trial Expansion: MAIA Biotechnology has announced the expansion of its Phase 2 THIO-101 trial for Ateganosine to a second clinical testing site in the U.S., aiming to treat non-small cell lung cancer and further validate the drug's clinical potential.
- Innovative Drug Mechanism: As the first-in-class telomere-targeting agent, Ateganosine attacks cancer cell telomeres, triggering immune responses that lead to tumor regression, showcasing its application prospects in patients who have failed chemotherapy.
- Global Trial Network: The trial is currently ongoing across 44 global sites, including two in the U.S., with MAIA planning to enroll up to 300 patients at these sites to support its goal of seeking accelerated FDA approval.
- Market Performance: MAIA's stock is currently trading at $1.34, up 3.47%, reflecting positive market sentiment regarding its clinical progress, which may pave the way for future financing and partnership opportunities.
See More
MAIA Biotechnology Advances THIO-101 Expansion Trial with New Clinical Site
- Clinical Trial Expansion: MAIA Biotechnology has activated its second U.S. clinical site for the THIO-101 expansion trial, now ongoing at 44 active sites across the U.S. and Europe, demonstrating the company's strong execution in the non-small cell lung cancer treatment space.
- Significant Market Potential: The potential breakthrough therapy of THIO-101 holds a substantial position in the projected $70 billion global non-small cell lung cancer market, indicating MAIA's strategic significance in the cancer immunotherapy landscape.
- Enhanced Patient Recruitment Efficiency: By broadening its clinical trial site footprint, MAIA can recruit patients more efficiently, advancing the program under FDA Fast Track designation and moving towards upcoming interim data milestones.
- Global Regulatory Approvals: MAIA has received regulatory approval to screen patients in Taiwan, Turkey, and select European countries, further expanding its clinical trial's international reach and enhancing its competitive edge in the global market.
See More
MAIA Biotechnology Updates on Phase 3 Trial Progress
- Clinical Trial Progress: MAIA Biotechnology has dosed 29 patients in its pivotal Phase 3 trial THIO-104 across 34 activated sites in six countries, demonstrating early momentum and targeting up to 100 patients by year-end to provide sufficient survival data for an interim analysis in 2027.
- FDA Fast Track Designation: The U.S. FDA has granted Fast Track designation for Ateganosine as a third-line treatment for NSCLC, and if Phase 3 data aligns with Phase 2 THIO-101 trial results, the company anticipates full approval for Ateganosine, enhancing its market position.
- Market Opportunity Assessment: MAIA views Ateganosine as having significant commercial potential in the projected $70 billion global NSCLC treatment market by 2030, indicating a positive outlook for the drug's market prospects and potential revenue growth.
- Stock Price Fluctuation: MAIA's stock has traded between $0.87 and $3.19 over the past year, closing at $1.50 with a 4.90% increase on Thursday, although it fell 1.33% to $1.48 in after-hours trading, reflecting market caution regarding its clinical progress.
See More
MAIA's Novel Telomere Therapy Shows Strong Progress in Lung Cancer Trial
- Trial Progress: MAIA's THIO-104 Phase 3 trial has dosed 29 patients across 34 sites in 6 countries, demonstrating strong enrollment momentum, with a target of 100 patients by year-end and potential interim analysis in 2027.
- Survival Rate Comparison: The median overall survival for MAIA's lead therapy, ateganosine, was 17.8 months in the Phase 2 trial, compared to only 5.8 months for standard chemotherapy, indicating a significant therapeutic advantage.
- Market Potential: As the first telomere-targeting therapy, ateganosine is projected to tap into a $70 billion global NSCLC market by 2030, presenting substantial commercial opportunities.
- FDA Fast Track Designation: The FDA has granted ateganosine Fast Track designation, expediting its approval process as a third-line treatment for NSCLC, thereby enhancing its competitive positioning in the market.
See More
MAIA Biotechnology Receives FDA Approval for Phase 2 Trial Expansion
- FDA Trial Expansion Approval: MAIA Biotechnology announced that the FDA has cleared its IND amendment to commence U.S. enrollment for the expansion of the Phase 2 THIO-101 trial, aimed at evaluating Ateganosine's efficacy in lung cancer treatment.
- Enhanced Manufacturing Efficiency: The FDA's clearance is supported by updated manufacturing efficiencies, including new manufacturers and formulation/storage conditions for Ateganosine, which will help improve drug production capacity and quality.
- Clinical Trial Design: The THIO-101 trial is designed to evaluate Ateganosine's anti-tumor activity, with primary objectives to assess its safety and tolerability, using Overall Response Rate (ORR) as the primary clinical endpoint, particularly targeting patients resistant to checkpoint inhibitors and chemotherapy.
- Accelerated Approval Potential: MAIA stated that additional data from the THIO-101 expansion study may further support a filing for FDA Accelerated Approval, enhancing the company's position in the competitive biopharmaceutical market.
See More
MAIA Biotechnology Expands THIO-101 Trial with FDA Approval
- FDA IND Update Approval: MAIA Biotechnology has received FDA clearance to update its investigational new drug (IND) application, allowing the expansion of the THIO-101 trial in the U.S. for treating advanced non-small cell lung cancer (NSCLC), marking a significant advancement in its clinical trial efforts.
- Trial Expansion: The THIO-101 study plans to add up to five clinical sites in the U.S., with the first site activated at Summit Medical Group in New Jersey, which is expected to significantly enhance patient recruitment efficiency and accelerate research progress.
- Positive Survival Data: So far, eight patients treated with ateganosine in Parts A and B of THIO-101 have shown overall survival (OS) beyond two years, providing a solid foundation for the evaluations in Parts C and D, particularly in the urgent third-line treatment area where improved clinical outcomes are critically needed.
- Fast Track Designation: The FDA granted ateganosine Fast Track designation in July 2025, allowing for more frequent communication and potential Accelerated Approval, which will help MAIA rapidly introduce its innovative therapy in the competitive NSCLC treatment market.
See More
MAIA Biotechnology Expands Phase 2 Trial for Ateganosine
- Trial Expansion: MAIA Biotechnology has announced the expansion of its Phase 2 THIO-101 trial for Ateganosine to a second clinical testing site in the U.S., aiming to treat non-small cell lung cancer and further validate the drug's clinical potential.
- Innovative Drug Mechanism: As the first-in-class telomere-targeting agent, Ateganosine attacks cancer cell telomeres, triggering immune responses that lead to tumor regression, showcasing its application prospects in patients who have failed chemotherapy.
- Global Trial Network: The trial is currently ongoing across 44 global sites, including two in the U.S., with MAIA planning to enroll up to 300 patients at these sites to support its goal of seeking accelerated FDA approval.
- Market Performance: MAIA's stock is currently trading at $1.34, up 3.47%, reflecting positive market sentiment regarding its clinical progress, which may pave the way for future financing and partnership opportunities.
See More
MAIA Biotechnology Advances THIO-101 Expansion Trial with New Clinical Site
- Clinical Trial Expansion: MAIA Biotechnology has activated its second U.S. clinical site for the THIO-101 expansion trial, now ongoing at 44 active sites across the U.S. and Europe, demonstrating the company's strong execution in the non-small cell lung cancer treatment space.
- Significant Market Potential: The potential breakthrough therapy of THIO-101 holds a substantial position in the projected $70 billion global non-small cell lung cancer market, indicating MAIA's strategic significance in the cancer immunotherapy landscape.
- Enhanced Patient Recruitment Efficiency: By broadening its clinical trial site footprint, MAIA can recruit patients more efficiently, advancing the program under FDA Fast Track designation and moving towards upcoming interim data milestones.
- Global Regulatory Approvals: MAIA has received regulatory approval to screen patients in Taiwan, Turkey, and select European countries, further expanding its clinical trial's international reach and enhancing its competitive edge in the global market.
See More
MAIA Biotechnology Updates on Phase 3 Trial Progress
- Clinical Trial Progress: MAIA Biotechnology has dosed 29 patients in its pivotal Phase 3 trial THIO-104 across 34 activated sites in six countries, demonstrating early momentum and targeting up to 100 patients by year-end to provide sufficient survival data for an interim analysis in 2027.
- FDA Fast Track Designation: The U.S. FDA has granted Fast Track designation for Ateganosine as a third-line treatment for NSCLC, and if Phase 3 data aligns with Phase 2 THIO-101 trial results, the company anticipates full approval for Ateganosine, enhancing its market position.
- Market Opportunity Assessment: MAIA views Ateganosine as having significant commercial potential in the projected $70 billion global NSCLC treatment market by 2030, indicating a positive outlook for the drug's market prospects and potential revenue growth.
- Stock Price Fluctuation: MAIA's stock has traded between $0.87 and $3.19 over the past year, closing at $1.50 with a 4.90% increase on Thursday, although it fell 1.33% to $1.48 in after-hours trading, reflecting market caution regarding its clinical progress.
See More
MAIA's Novel Telomere Therapy Shows Strong Progress in Lung Cancer Trial
- Trial Progress: MAIA's THIO-104 Phase 3 trial has dosed 29 patients across 34 sites in 6 countries, demonstrating strong enrollment momentum, with a target of 100 patients by year-end and potential interim analysis in 2027.
- Survival Rate Comparison: The median overall survival for MAIA's lead therapy, ateganosine, was 17.8 months in the Phase 2 trial, compared to only 5.8 months for standard chemotherapy, indicating a significant therapeutic advantage.
- Market Potential: As the first telomere-targeting therapy, ateganosine is projected to tap into a $70 billion global NSCLC market by 2030, presenting substantial commercial opportunities.
- FDA Fast Track Designation: The FDA has granted ateganosine Fast Track designation, expediting its approval process as a third-line treatment for NSCLC, thereby enhancing its competitive positioning in the market.
See More
MAIA Biotechnology Receives FDA Approval for Phase 2 Trial Expansion
- FDA Trial Expansion Approval: MAIA Biotechnology announced that the FDA has cleared its IND amendment to commence U.S. enrollment for the expansion of the Phase 2 THIO-101 trial, aimed at evaluating Ateganosine's efficacy in lung cancer treatment.
- Enhanced Manufacturing Efficiency: The FDA's clearance is supported by updated manufacturing efficiencies, including new manufacturers and formulation/storage conditions for Ateganosine, which will help improve drug production capacity and quality.
- Clinical Trial Design: The THIO-101 trial is designed to evaluate Ateganosine's anti-tumor activity, with primary objectives to assess its safety and tolerability, using Overall Response Rate (ORR) as the primary clinical endpoint, particularly targeting patients resistant to checkpoint inhibitors and chemotherapy.
- Accelerated Approval Potential: MAIA stated that additional data from the THIO-101 expansion study may further support a filing for FDA Accelerated Approval, enhancing the company's position in the competitive biopharmaceutical market.
See More
MAIA Biotechnology Expands THIO-101 Trial with FDA Approval
- FDA IND Update Approval: MAIA Biotechnology has received FDA clearance to update its investigational new drug (IND) application, allowing the expansion of the THIO-101 trial in the U.S. for treating advanced non-small cell lung cancer (NSCLC), marking a significant advancement in its clinical trial efforts.
- Trial Expansion: The THIO-101 study plans to add up to five clinical sites in the U.S., with the first site activated at Summit Medical Group in New Jersey, which is expected to significantly enhance patient recruitment efficiency and accelerate research progress.
- Positive Survival Data: So far, eight patients treated with ateganosine in Parts A and B of THIO-101 have shown overall survival (OS) beyond two years, providing a solid foundation for the evaluations in Parts C and D, particularly in the urgent third-line treatment area where improved clinical outcomes are critically needed.
- Fast Track Designation: The FDA granted ateganosine Fast Track designation in July 2025, allowing for more frequent communication and potential Accelerated Approval, which will help MAIA rapidly introduce its innovative therapy in the competitive NSCLC treatment market.
See More
