Gannet BioChem Partners with Serina Therapeutics for SER-252 Development
Written by Emily J. Thompson, Senior Investment Analyst
Updated: Jun 30 2026
0mins
Source: Newsfilter
- Drug Development Partnership: Gannet BioChem has entered into a partnership with Serina Therapeutics to support the development of SER-252, an investigational therapy for advanced Parkinson's disease, highlighting strategic collaboration in the biopharmaceutical sector.
- FDA Approval Accelerates Clinical Progress: SER-252 recently received FDA clearance for its Investigational New Drug (IND) application, enabling its advancement into clinical development, which is expected to expedite the path to market for this innovative therapy.
- Complementary Technical Expertise: The collaboration leverages Serina's proprietary POZ Platform™ technology alongside Gannet's expertise in process development and manufacturing support for complex therapeutic programs, aiming to enhance drug delivery efficiency and safety profiles.
- Expanded Industry Influence: Gannet BioChem's participation in the 2026 BIO International Convention further solidifies its influence in the biopharmaceutical industry and lays the groundwork for future collaboration opportunities.
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Analyst Views on SER
Wall Street analysts forecast SER stock price to rise
1 Analyst Rating
1 Buy
0 Hold
0 Sell
Moderate Buy
Current: 2.170
Low
11.00
Averages
11.00
High
11.00
Current: 2.170
Low
11.00
Averages
11.00
High
11.00
About SER
Serina Therapeutics Inc. is a clinical-stage biotechnology company developing a pipeline of wholly owned drug product candidates to treat neurological diseases and other indications. The Company's POZ Platform provides the potential to improve the integrated efficacy and safety profile of multiple modalities including small molecules, RNA-based therapeutics and antibody-based drug conjugates (ADCs). Its proprietary POZ technology is based on a synthetic, water soluble, low viscosity polymer called poly(2-oxazoline). Its POZ technology is engineered to provide greater control in drug loading and more precision in the rate of release of attached drugs delivered via subcutaneous injection. SER-252 is the Company’s lead candidate for advanced Parkinson’s disease. SER-252 is an investigational apomorphine therapy developed with its POZ platform and designed to provide continuous dopaminergic stimulation.
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.
Gannet BioChem Partners with Serina Therapeutics for SER-252 Development
- Development Partnership: Gannet BioChem has entered into a collaboration with clinical-stage biotech Serina Therapeutics to support the development of SER-252, an investigational therapy for advanced Parkinson's disease, highlighting a strategic alliance in the biopharmaceutical sector.
- FDA Approval Milestone: The investigational new drug (IND) application for SER-252 has been cleared by the U.S. FDA, paving the way for the advancement of its clinical program and indicating the therapy's market potential.
- Combined Technological Strengths: This partnership integrates Serina's proprietary POZ technology with Gannet BioChem's expertise in polymer process development and manufacturing, aiming to enhance product development efficiency and accelerate market entry.
- Market Performance Insight: Serina Therapeutics' stock has traded between $1.22 and $7.92 over the past year, closing at $1.94, and despite a slight recent decline, the outlook for the collaboration remains positive.
See More
Gannet BioChem Partners with Serina Therapeutics for SER-252 Development
- Drug Development Partnership: Gannet BioChem has entered into a partnership with Serina Therapeutics to support the development of SER-252, an investigational therapy for advanced Parkinson's disease, highlighting strategic collaboration in the biopharmaceutical sector.
- FDA Approval Accelerates Clinical Progress: SER-252 recently received FDA clearance for its Investigational New Drug (IND) application, enabling its advancement into clinical development, which is expected to expedite the path to market for this innovative therapy.
- Complementary Technical Expertise: The collaboration leverages Serina's proprietary POZ Platform™ technology alongside Gannet's expertise in process development and manufacturing support for complex therapeutic programs, aiming to enhance drug delivery efficiency and safety profiles.
- Expanded Industry Influence: Gannet BioChem's participation in the 2026 BIO International Convention further solidifies its influence in the biopharmaceutical industry and lays the groundwork for future collaboration opportunities.
See More
Serina Therapeutics Q1 Earnings Miss Expectations
- Earnings Miss: Serina Therapeutics reported a Q1 GAAP EPS of -$0.58, missing expectations by $0.14, indicating challenges in profitability that could impact investor confidence moving forward.
- Cash Position: As of March 31, 2026, the company had $24.5 million in cash and cash equivalents, which, while providing some liquidity, raises concerns about capital efficiency and future funding needs.
- PIPE Financing Update: In April 2026, Serina secured $5.2 million in gross proceeds from a PIPE financing completed in March 2026, which supports ongoing operations but necessitates evaluation of its long-term financial health implications.
- Listing Compliance Progress: The company received NYSE approval with a compliance deadline set for 2027, reflecting its commitment to regulatory adherence, which may facilitate future capital market activities.
See More
Serina Unveils Novel POZ Platform Lipid Nanoparticles
- Novel Lipid Nanoparticles: At the LNP Summit in Boston, Serina Therapeutics showcased novel lipid nanoparticles built on the POZ platform, which did not elicit an antibody response in a vaccine format, indicating potential safety advantages that could disrupt the current LNP formulation market.
- Replacement Strategy Progress: The company is advancing a replacement strategy targeting ionizable lipids, which have raised safety concerns, signaling Serina's ongoing commitment to enhancing the safety of LNP components and potentially boosting its competitive edge in the market.
- Versatile Drug Carriers: The newly designed polymer-lipid can bind a broad range of oligonucleotide payloads, demonstrating versatility and flexibility in drug delivery, which may provide new solutions for treating neurological diseases and expand the company's product pipeline.
- Strategic Partnership Opportunities: Serina intends to advance applications of the POZ platform through out-licensing and co-development, particularly highlighted by its non-exclusive licensing agreement with Pfizer, indicating a strategic positioning in the drug delivery sector that could lay the groundwork for future revenue growth.
See More
Serina Therapeutics Receives NYSE Compliance Plan Approval
- Compliance Plan Approved: Serina Therapeutics' business plan has been accepted by NYSE American LLC, granting the company until July 9, 2027, to regain compliance, demonstrating a proactive approach to regulatory challenges.
- Financial Condition Disclosure: As of December 31, 2024, Serina reported stockholders' equity of $1.6 million and incurred net losses in three of the last four fiscal years, with a net loss of $19.4 million in 2025, highlighting financial pressures and challenges to future profitability.
- Clinical Trial Progress: Serina is advancing its SER-252 clinical program, having enrolled and dosed its first patient in February 2026 for its registrational trial targeting advanced Parkinson's disease, indicating ongoing commitment to research and new therapies.
- Market Performance Analysis: SER stock has traded between $1.22 and $7.92 over the past year, closing at $2.12, with a recent overnight increase of 4.25% to $2.21, reflecting investor interest in the company's future developments.
See More
Serina Therapeutics Receives NYSE Approval to Regain Listing Compliance
- Compliance Plan Approved: Serina Therapeutics (SER) has received NYSE American approval for its plan to regain listing compliance after being flagged on January 9, 2026, due to low equity of $1.6 million and losses in three of the last four years, demonstrating the company's resilience in facing financial challenges.
- Grace Period Established: The company has until July 9, 2027, to meet the listing rules, providing Serina with the necessary time to improve its financial condition and avoid potential delisting risks.
- Quarterly Monitoring Mechanism: During the grace period, NYSE American will monitor Serina quarterly, and failure to meet listing requirements within the cure period may lead to suspension and delisting, which would directly impact shareholder confidence and market performance.
- Funding Opportunities: Serina Therapeutics has also secured up to $30 million in private placement, which will aid in improving its financial situation and support future business development, further enhancing its viability in the capital markets.
See More
Gannet BioChem Partners with Serina Therapeutics for SER-252 Development
- Development Partnership: Gannet BioChem has entered into a collaboration with clinical-stage biotech Serina Therapeutics to support the development of SER-252, an investigational therapy for advanced Parkinson's disease, highlighting a strategic alliance in the biopharmaceutical sector.
- FDA Approval Milestone: The investigational new drug (IND) application for SER-252 has been cleared by the U.S. FDA, paving the way for the advancement of its clinical program and indicating the therapy's market potential.
- Combined Technological Strengths: This partnership integrates Serina's proprietary POZ technology with Gannet BioChem's expertise in polymer process development and manufacturing, aiming to enhance product development efficiency and accelerate market entry.
- Market Performance Insight: Serina Therapeutics' stock has traded between $1.22 and $7.92 over the past year, closing at $1.94, and despite a slight recent decline, the outlook for the collaboration remains positive.
See More
Gannet BioChem Partners with Serina Therapeutics for SER-252 Development
- Drug Development Partnership: Gannet BioChem has entered into a partnership with Serina Therapeutics to support the development of SER-252, an investigational therapy for advanced Parkinson's disease, highlighting strategic collaboration in the biopharmaceutical sector.
- FDA Approval Accelerates Clinical Progress: SER-252 recently received FDA clearance for its Investigational New Drug (IND) application, enabling its advancement into clinical development, which is expected to expedite the path to market for this innovative therapy.
- Complementary Technical Expertise: The collaboration leverages Serina's proprietary POZ Platform™ technology alongside Gannet's expertise in process development and manufacturing support for complex therapeutic programs, aiming to enhance drug delivery efficiency and safety profiles.
- Expanded Industry Influence: Gannet BioChem's participation in the 2026 BIO International Convention further solidifies its influence in the biopharmaceutical industry and lays the groundwork for future collaboration opportunities.
See More
Serina Therapeutics Q1 Earnings Miss Expectations
- Earnings Miss: Serina Therapeutics reported a Q1 GAAP EPS of -$0.58, missing expectations by $0.14, indicating challenges in profitability that could impact investor confidence moving forward.
- Cash Position: As of March 31, 2026, the company had $24.5 million in cash and cash equivalents, which, while providing some liquidity, raises concerns about capital efficiency and future funding needs.
- PIPE Financing Update: In April 2026, Serina secured $5.2 million in gross proceeds from a PIPE financing completed in March 2026, which supports ongoing operations but necessitates evaluation of its long-term financial health implications.
- Listing Compliance Progress: The company received NYSE approval with a compliance deadline set for 2027, reflecting its commitment to regulatory adherence, which may facilitate future capital market activities.
See More
Serina Unveils Novel POZ Platform Lipid Nanoparticles
- Novel Lipid Nanoparticles: At the LNP Summit in Boston, Serina Therapeutics showcased novel lipid nanoparticles built on the POZ platform, which did not elicit an antibody response in a vaccine format, indicating potential safety advantages that could disrupt the current LNP formulation market.
- Replacement Strategy Progress: The company is advancing a replacement strategy targeting ionizable lipids, which have raised safety concerns, signaling Serina's ongoing commitment to enhancing the safety of LNP components and potentially boosting its competitive edge in the market.
- Versatile Drug Carriers: The newly designed polymer-lipid can bind a broad range of oligonucleotide payloads, demonstrating versatility and flexibility in drug delivery, which may provide new solutions for treating neurological diseases and expand the company's product pipeline.
- Strategic Partnership Opportunities: Serina intends to advance applications of the POZ platform through out-licensing and co-development, particularly highlighted by its non-exclusive licensing agreement with Pfizer, indicating a strategic positioning in the drug delivery sector that could lay the groundwork for future revenue growth.
See More
Serina Therapeutics Receives NYSE Compliance Plan Approval
- Compliance Plan Approved: Serina Therapeutics' business plan has been accepted by NYSE American LLC, granting the company until July 9, 2027, to regain compliance, demonstrating a proactive approach to regulatory challenges.
- Financial Condition Disclosure: As of December 31, 2024, Serina reported stockholders' equity of $1.6 million and incurred net losses in three of the last four fiscal years, with a net loss of $19.4 million in 2025, highlighting financial pressures and challenges to future profitability.
- Clinical Trial Progress: Serina is advancing its SER-252 clinical program, having enrolled and dosed its first patient in February 2026 for its registrational trial targeting advanced Parkinson's disease, indicating ongoing commitment to research and new therapies.
- Market Performance Analysis: SER stock has traded between $1.22 and $7.92 over the past year, closing at $2.12, with a recent overnight increase of 4.25% to $2.21, reflecting investor interest in the company's future developments.
See More
Serina Therapeutics Receives NYSE Approval to Regain Listing Compliance
- Compliance Plan Approved: Serina Therapeutics (SER) has received NYSE American approval for its plan to regain listing compliance after being flagged on January 9, 2026, due to low equity of $1.6 million and losses in three of the last four years, demonstrating the company's resilience in facing financial challenges.
- Grace Period Established: The company has until July 9, 2027, to meet the listing rules, providing Serina with the necessary time to improve its financial condition and avoid potential delisting risks.
- Quarterly Monitoring Mechanism: During the grace period, NYSE American will monitor Serina quarterly, and failure to meet listing requirements within the cure period may lead to suspension and delisting, which would directly impact shareholder confidence and market performance.
- Funding Opportunities: Serina Therapeutics has also secured up to $30 million in private placement, which will aid in improving its financial situation and support future business development, further enhancing its viability in the capital markets.
See More
