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Adagene Inc. (Nasdaq: ADAG) is a platform-driven, clinical-stage biotechnology company specializing in the discovery and development of novel antibody-based cancer immunotherapies. Co-founded by two serial entrepreneurs, Adagene aims to become a leader in antibody discovery and engineering. The company has developed a proprietary Dynamic Precision Library (DPL), showcasing its capabilities through a unique pipeline of innovative antibody therapeutics advancing into clinical trials.
The company's proprietary technologies, including NEObody™, SAFEbody®, and POWERbody™, enable the design of therapeutic antibody candidates with functional epitopes and cross-reactivity across species. These innovations are particularly focused on cancer immunotherapy, where Adagene’s pipeline features monoclonal antibody drugs targeting various cancers.
Adagene has raised over $86 million through three series of financing, with significant investments from F-Prime Capital, Eight Roads Ventures China, 6 Dimensions Capital, GP Healthcare Capital, Sequoia China, and New World TMT. The company utilizes computational biology and artificial intelligence to address unmet patient needs, striving to transform the discovery and development of therapies with enhanced safety and efficacy profiles.
One of Adagene’s key advancements is the development of ADG126, a masked anti-CTLA-4 SAFEbody, which is currently in clinical trials. Recent data highlighted no dose-limiting toxicities and compelling safety when combined with anti-PD-1 therapy. The results indicated tumor shrinkage in cold tumors and partial responses in multiple tumor types. Another notable candidate, ADG116, an unmasked anti-CTLA-4 NEObody, has also shown promising safety and anti-tumor activity in clinical trials.
Adagene’s strategic collaborations with global biopharmaceutical companies, including Roche, Sanofi, and Exelixis, emphasize the commercial potential of its antibody technologies. These partnerships leverage Adagene's platform for developing advanced therapies, including antibody-drug conjugates and bispecific antibodies, addressing a wide range of cancer types.
Financially, Adagene reported a cash balance of $143.8 million at the end of 2022, supporting streamlined operations into 2025. The company continues to prioritize its clinical programs and collaborations, aiming to maximize the therapeutic potential of its proprietary technologies.
For more information, please visit Adagene’s investor website.
Adagene Inc. (Nasdaq: ADAG) has showcased the promising results of its drug ADG126 at the ESMO Congress 2022. Interim data from an ongoing Phase 1/2 trial indicates that ADG126, an innovative anti-CTLA-4 SAFEbody®, demonstrates a solid safety profile with no significant adverse effects reported at doses up to 20 mg/kg. Notably, antitumor activity was observed in cold tumors, highlighted by a patient with ovarian cancer showing a 90% drop in the biomarker CA125. Ongoing trials aim to further evaluate ADG126 in combination with anti-PD-1 therapies.
Adagene Inc. (Nasdaq: ADAG) reported positive topline results for its anti-CTLA-4 antibody, ADG116, showing safety and clinical responses in combination with anti-PD-1 therapy. Regulatory filing for ADG206's clinical trial is underway, with patient dosing planned for early 2023. Financially, the company holds US$168 million in cash, sufficient to support operations into late 2024. Notably, net revenue increased to US$3.9 million for H1 2022, rising from US$1.4 million in 2021, aided by collaborations with Sanofi and Exelixis.
Adagene Inc. (Nasdaq: ADAG) announced a share repurchase program allowing up to US$10 million in buybacks of its ordinary shares. This 2022 Share Repurchase Program enables Adagene to repurchase shares at prevailing market prices through various means, subject to market conditions and regulatory requirements. The program will commence upon agreement with a broker-dealer and lasts for twelve months. Adagene aims to utilize existing funds for this initiative, signaling confidence in its share value and long-term market strategy.
Adagene Inc. (Nasdaq: ADAG) announced promising interim results for its anti-CTLA-4 monoclonal antibody, ADG126, at the ASCO 2022 meeting. The ongoing Phase 1 trial shows no dose-limiting toxicities and only mild treatment-related adverse events in 16 heavily pretreated patients. Two patients demonstrated significant tumor reduction, with one experiencing a 77% decrease in CA-125 levels. Adagene aims to confirm ADG126's safety in combination with anti-PD-1 therapies in upcoming analyses while continuing dose escalation and expansion in the study.
Adagene Inc. (Nasdaq: ADAG) will participate in several upcoming investor conferences, including a live Fireside Chat at the Jefferies Global Healthcare Conference on June 8 at 4:30 p.m. ET and one-on-one meetings at the Goldman Sachs Annual Global Healthcare Conference on June 13. Additionally, Adagene will engage in virtual meetings during the ICA 2nd Annual Asia Pacific Healthcare Conference from May 18-24 and the Berenberg Emerging Biotech Conference on May 19. The company focuses on developing novel antibody-based cancer immunotherapies utilizing advanced technologies.
Adagene Inc. (Nasdaq: ADAG) presented promising preclinical data at the AACR Annual Meeting 2022, showcasing its new antibody candidates designed for improved cancer therapy. The showcased candidates include ADG206, a masked anti-CD137 therapy, ADG153, a masked anti-CD47 antibody, and ADG138, a HER2×CD3 bispecific T-cell engager. All candidates incorporate SAFEbody technology for enhanced safety and efficacy. IND filings for ADG206 and ADG153 are expected in 2022, marking a significant milestone towards advancing these innovative therapies.
Adagene Inc. (ADAG) reported significant advancements in its pipeline, focusing on anti-CTLA-4 programs ADG116 and ADG126. The company established a strategic collaboration with Sanofi valued at over $2.5 billion, enhancing its SAFEbody technology platform. For 2021, net revenue surged to $10.2 million from $0.7 million in 2020, bolstered by licensing agreements. Despite a net loss of $73.2 million attributable to increased R&D expenses, Adagene maintains a strong cash position of $174.4 million, supporting its ambitious development plans for 2022.
Adagene Inc. (Nasdaq: ADAG) has received FDA clearance to initiate a Phase 1b/2 clinical trial for its anti-CTLA-4 monoclonal antibody, ADG126, in combination with pembrolizumab. The ADG126-P001 trial will take place at multiple sites in the U.S. and Asia Pacific and aims to treat patients with advanced solid tumors. ADG126 utilizes SAFEbody technology for enhanced targeting in the tumor microenvironment, aiming to improve safety and efficacy profiles. The trial is set to begin soon with a focus on dose escalation and early efficacy evaluation.
Adagene Inc. (Nasdaq: ADAG) announced advancements in its cancer immunotherapy pipeline, revealing four abstracts for the AACR Annual Meeting 2022. These presentations detail promising preclinical data for three product candidates: ADG138, ADG206, and ADG153. Utilizing its AI-driven platform, Adagene aims to enhance safety and efficacy through POWERbody technology, integrating SAFEbody® precision masking. Findings suggest effective immunotherapy for solid tumors via innovative approaches in antibody development. The meeting takes place from April 8-13, 2022, in New Orleans.
Adagene Inc. (Nasdaq: ADAG) has announced a collaboration and exclusive licensing agreement with Sanofi for the development of masked monoclonal and bispecific antibodies.
Sanofi will pay Adagene $17.5 million upfront and could lead to potential milestone payments totaling $2.5 billion. Adagene will focus on early-stage research using its SAFEbody technology, which targets tumors while minimizing toxicity. This partnership aims to address unmet needs in oncology, leveraging Adagene's AI-driven platform and extensive preclinical research.
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