Adagene Inc. develops antibody-based cancer immunotherapies as a Nasdaq-listed foreign issuer whose securities trade as ADSs under ADAG. The company uses computational biology and artificial intelligence through its proprietary Dynamic Precision Library platform, including NEObody, SAFEbody and POWERbody technologies, to design masked and engineered antibody programs.
Recurring company updates center on muzastotug (ADG126), a masked anti-CTLA-4 SAFEbody, clinical data in microsatellite stable colorectal cancer and hepatocellular carcinoma, combination studies with checkpoint and bispecific therapies, and FDA Fast Track designation in MSS metastatic colorectal cancer. Other developments include scientific meeting presentations, SAFEbody collaborations and licensing, advisory board changes, financial results and ADS capital offerings.
Adagene Inc. (Nasdaq: ADAG) has initiated a phase 1b/2 clinical trial for ADG106, an anti-CD137 agonist antibody combined with nivolumab for advanced non-small cell lung cancer (NSCLC) patients. The trial, conducted in Singapore, aims to evaluate safety, tolerability, and efficacy in 53 patients who have progressed after prior treatments. Dr. Peter Luo mentioned the trial's potential to address resistance to anti-PD-1 therapy. This development is crucial, given that metastatic NSCLC is a leading cause of cancer-related deaths worldwide.
Adagene Inc. (Nasdaq: ADAG) announced a $3 million milestone payment triggered by the successful nomination of lead SAFEbody candidates in collaboration with Exelixis. This milestone underscores the efficacy of Adagene's SAFEbody precision masking technology in developing antibody-drug conjugates. The collaboration also included an upfront payment of $11 million and eligibility for further commercialization milestones and royalties. Adagene's pipeline includes several clinical-stage programs, with ongoing trials validating its SAFEbody technology in treating cancer.
Adagene (Nasdaq: ADAG) presented preclinical data at the 63rd American Society of Hematology Annual Meeting, highlighting two promising programs: ADG153, an anti-CD47 monoclonal antibody, and ADG152, a CD20xCD3 bispecific T-cell engager. ADG153 demonstrated reduced hematologic toxicities and an 8-fold prolonged half-life, while ADG152 showcased enhanced therapeutic index with minimized cytokine release. These findings support advancing both candidates into clinical development, showcasing Adagene's commitment to innovative cancer immunotherapies and the strength of its AI-driven antibody platform.
Adagene Inc. has presented promising clinical data on its anti-CTLA-4 monoclonal antibody ADG116 and anti-CD137 agonist ADG106 at the ESMO-IO Congress 2021. ADG116 showed a strong safety profile and early efficacy signals in patients with advanced solid tumors, with a notable 22% tumor reduction in a pancreatic cancer patient. Additionally, ADG106 demonstrated significant synergy with toripalimab, enhancing immune activation. These findings reinforce Adagene's commitment to developing innovative antibody-based immunotherapies and advancing its clinical pipeline.
Adagene presented promising clinical data for its monoclonal antibodies, ADG116 and ADG106, at the ESMO-IO Congress 2021. The ongoing trial of ADG116 indicated a strong safety profile with early efficacy signals in treatment-resistant tumors. Key findings included a 22% reduction in tumor size for a pancreatic cancer patient and evidence of immune activation. ADG106 showed enhanced immune response when combined with toripalimab. The trials aim to advance these therapies targeting advanced solid tumors, reinforcing Adagene's commitment to innovative cancer treatments.
Adagene has received FDA clearance for the IND application to initiate the Phase 1b/2 clinical trial of its anti-CTLA-4 monoclonal antibody, ADG116, in combination with pembrolizumab. The global study (ADG116-P001) will target advanced metastatic solid tumors and will commence in early 2022 across multiple sites in the U.S. and Asia Pacific. This trial aims to evaluate safety, tolerability, and preliminary efficacy. Additionally, the ongoing ADG116-1003 trial will explore ADG116 in combinations with other therapies.
Adagene Inc. (Nasdaq: ADAG) announced two poster presentations at the ESMO-IO Congress 2021 showcasing clinical data for its anti-CD137 agonist, ADG106, and anti-CTLA-4 monoclonal antibody, ADG116. The data highlight the potential of the NEObody™ technology in improving T-cell activation and safety profiles in cancer immunotherapy. Key presentations include biomarker kinetics for ADG106 and a dose-finding study for ADG116. The conference takes place from December 8-11, 2021, with details available after December 2.
Adagene Inc. (Nasdaq: ADAG) announced its participation in several investor and industry conferences throughout November 2021. Key events include one-on-one meetings during the Goldman Sachs Asia Pacific Healthcare Forum from November 15-17, its presentation at the 8th Annual BioCentury-BayHelix China Healthcare Summit from November 16-19, and on-demand viewing of its presentation at the Jefferies London Healthcare Conference starting November 18. Additionally, an on-demand presentation for the Piper Sandler 33rd Annual Virtual Healthcare Conference will be available from November 22.
Adagene Inc. (Nasdaq: ADAG) announced the presentation of promising preclinical data for its antibody candidates ADG153 (anti-CD47 SAFEbody) and ADG152 (CD20xCD3 POWERbody). These candidates aim to tackle development challenges in immuno-oncology. Notable performance includes ADG153's strong anti-tumor activity with minimal liabilities and ADG152 showing an enhanced therapeutic index. The results will be presented at the ASH Annual Meeting in December 2021, with implications for potential Investigational New Drug applications.
Adagene has initiated a phase 1b/2 clinical trial of ADG106, an anti-CD137 agonist antibody, in combination with Nivolumab, targeting advanced non-small cell lung cancer (NSCLC). Conducted at the National University Cancer Institute, Singapore, this trial aims to evaluate safety, tolerability, and anti-tumor efficacy in up to 53 patients who have failed prior treatments. The promising pre-clinical results suggest potential for ADG106 to enhance T-cell activity and address resistance to current therapies.