ASCENTAGE PHARMA GROUP INTERNATIONAL

ASCENTAGE PHARMA GROUP INTERNATIONAL (AAPG) Market Cap

ASCENTAGE PHARMA GROUP INTERNATIONAL has a market capitalization of $1.60B.

Price: $17.20

ā–¼ -1.08 (-5.91%)

Market Cap: 1.60B

NASDAQ Ā· time unavailable

CEO: Dajun Yang

Sector: Healthcare

Industry: Biotechnology

IPO Date: 2025-01-24

Website: https://www.ascentage.cn

ASCENTAGE PHARMA GROUP INTERNATIONAL (AAPG) - Company Information

Market Cap: 1.60B|Sector: Healthcare

Company Profile

Ascentage Pharma Group International, a clinical-stage biotechnology company, develops therapies for cancers, chronic hepatitis B virus (HBV), and age-related diseases in Mainland China. The company's primary product candidate is HQP1351, a BCR-ABL inhibitor targeting BCR-ABL1 mutants, including those with the T315I mutation. It also develops APG-2575, an oral administered Bcl-2 selective inhibitor for hematologic malignancies and solid tumors; APG-115, an oral small molecule inhibitor of the MDM2-p53 protein-protein interactions to treat solid tumors and hematological malignancies; and APG-1252, a small molecule drug to restore apoptosis through dual inhibition of the Bcl-2 and Bcl-xL proteins for the treatment of small-cell lung cancer, non-small cell lung cancer, neuroendocrine tumor, and non-Hodgkin's lymphoma. In addition, the company is developing APG-1387, a small molecule inhibitor of apoptosis proteins for advanced solid tumors and chronic HBV infection; APG-2449, an oral inhibitor of FAK, ROS1, and ALK kinases; APG-5918, an orally available and selective embryonic ectoderm development inhibitor; APG-265, a MDM2 protein degrader; and UBX1967/1325, which are Bcl-2 inhibitors. In addition, it is also involved in medical research and development; clinical development; clinical trial operation; venture capital investment; rental services; and science and technology promotion services. The company has collaboration relationships with biotechnology and pharmaceutical companies; and research institutions. Ascentage Pharma Group International was founded in 2009 and is headquartered in Suzhou, China.

Analyst Sentiment

92%
Strong Buy

From 1 Active Polls

1Y Forecast: $40.00

ā–² +132.6% Potential Upside

Consensus Target Metrics

Low Bound

$40

Median

$40

High Bound

$40

Average

$40

Price & Moving Averages

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šŸŽÆ Wall Street Analyst Intelligence Report

1-Year structural target targets, chart projections, and sentiment maps.

Average 1Y Target
$40.00
ā–² +132.56% Upside
Low Target
$40.00
133% Risk
Median Target
$40.00
133% Mid
High Target
$40.00
133% Max
Consensus
Buy
1 / 1 Buys

Consensus Trend Projection

Trailing closures vs. 12-month metrics map.

Analyst Vote Distribution

Aggregate institutional coverage sentiment weights.

šŸ“Š Historical Valuation Multiples

Real-time Trailing Twelve Month (TTM) momentum side-by-side with discrete quarterly metrics.

Fiscal QuarterTTMQ4 2025Q2 2025Q4 2024Q2 2024Q4 2023Q2 2023Q4 2022Q2 2022
Period EndingTrailing 12MDec 31, 2025Jun 30, 2025Dec 31, 2024Jun 30, 2024Dec 31, 2023Jun 30, 2023Dec 31, 2022Jun 30, 2022
Market Cap ($M)1,59916,99124,0829,9069,3598,9442,2241,9751,919
Enterprise Value ($M)10,33016,50124,13610,3389,9599,6712,3182,2931,781
Price to Earnings Ratio (P/E)-8.76-6.64-10.19-4.3614.35-4.27-1.38-1.12-1.09
Price/Earnings-to-Growth Ratio (PEG)—-0.15-0.21—0.02—-0.04—-0.00
Price to Sales Ratio (P/S)19.0650.85103.0563.1411.36112.8115.5818.8418.30
Price to Book Ratio (P/B)8.1312.8236.1637.5012.21148.043.774.832.19
Price to Free Cash Flow Ratio (P/FCF)-8.73-21.58-53.2642.11-25.23-24.19-5.38-4.43-4.31
Enterprise Value to Sales (EV/Sales)—49.38103.2865.8912.09121.9816.2421.8616.99
Enterprise Value to EBITDA (EV/EBITDA)-9.28-27.55-46.96-19.5643.38-19.63-9.24-5.56-4.32
Debt to Equity Ratio0.441.492.586.322.2229.722.844.391.78
āš ļø

Valuation Model Suspended

API Payload Error: Inverted or negative baseline Free Cash Flow margin detected (-105.8%).

Troubleshooting Notice: The upstream financial data supplier has uploaded corrupted or inverted baseline metrics for AAPG. The server sandbox cannot calculate an intrinsic value path from negative cash generation baselines.

šŸ“˜ Full Research Report

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AI-Generated Research: This report is for informational purposes only.

šŸ“˜ ASCENTAGE PHARMA GROUP INTERNATIONAL (AAPG) — Investment Overview

🧩 Business Model Overview

ASCENTAGE PHARMA GROUP INTERNATIONAL (AAPG) is positioned as a life-sciences and pharmaceutical-focused group operating across parts of the value chain that typically include (i) sourcing or developing therapeutics, (ii) navigating regulatory pathways, and (iii) commercializing products through distribution, partnerships, and/or direct go-to-market activities. In business-model terms, the investment case generally depends on where AAPG sits on the spectrum between ā€œresearch-led value creationā€ (pipeline development that later becomes commercially monetizable products) and ā€œcommercial-led value captureā€ (marketing/distribution and commercialization of approved therapies).

For investment evaluation, it is helpful to map AAPG’s model into three overlapping engines:

  • Product origination & lifecycle management: identifying candidate compounds or products, securing rights, advancing development where applicable, and extending product value through new indications, formulations, or geographic expansion.
  • Regulatory & commercialization capabilities: capability to secure approvals (directly or via partners) and execute commercial rollout—often including local registrations, quality systems, and supply chain reliability.
  • Partnering & monetisation structures: licensing, co-development, distribution agreements, or commercial partnerships that convert technical assets into cash flows while managing development risk and capital intensity.

Because companies in this sector can be structured very differently (asset-heavy pipeline developer vs. asset-light distributor vs. hybrid), the most important diligence step is to verify: (a) what percentage of value is tied to proprietary products/patents versus third-party rights, (b) the durability of revenue streams (recurring repeatable demand versus one-off shipments), and (c) whether margins are constrained primarily by COGS (manufacturing/sourcing) or by commercialization overhead (sales force, regulatory support, distribution).

šŸ’° Revenue Streams & Monetisation Model

AAPG’s monetisation model is most commonly built through a combination of product sales and contractual revenue mechanisms typical of pharma groups. Investors should think in terms of ā€œhow cash is generatedā€ rather than only ā€œhow revenue is reported.ā€ The core revenue streams to evaluate include:

  • Commercial product sales: revenue from the sale of pharmaceutical products, either through owned channels, distributor networks, hospitals/clinics, or via partner-led commercialization. Key margin drivers typically include procurement terms, manufacturing costs, logistics efficiency, and pricing power.
  • Licensing / royalties: revenue from licensing rights to third parties or earning royalties based on usage/sales. This structure can provide less operational risk than direct sales but depends heavily on partner execution and contract terms.
  • Distribution or service fees: revenue from acting as an intermediary for approved products, where the business economics often hinge on volume commitments, credit terms, and channel stability.
  • Development or milestone-based payments: revenue recognized from milestone events in partnerships. These can be lumpy and may not be reliable as a standalone base of recurring cash flows.

A robust investment view typically distinguishes between:

  • Recurring monetisation (product franchises with repeat demand, stable formularies, and predictable purchasing patterns), and
  • Event-driven monetisation (milestones, one-time approvals, or short-duration commercial ramps).

Given pharma group dynamics, the sustainability of margins is as important as revenue growth. Investors should scrutinize: (i) gross margin trajectory (COGS pressure vs. pricing improvements), (ii) working capital dynamics (inventory build, receivables collection), and (iii) contract structure (how much of the value accrues to AAPG versus manufacturing partners, distributors, and licensees). Even without using time-specific figures, the direction and drivers of these metrics matter for assessing whether AAPG can compound value across cycles.

🧠 Competitive Advantages & Market Positioning

Competitive advantage in pharma groups generally arises from a mix of commercial reach, regulatory execution, partner relationships, and asset/portfolio quality. For AAPG, the key question is whether its differentiators are structural (harder to replicate) or mostly transient (based on a favorable distribution contract or short-term pricing).

Potential areas of differentiation to evaluate include:

  • Regulatory and quality execution: the ability to maintain compliance across manufacturing, labeling, and distribution—reducing the risk of disruption, recalls, or approval delays.
  • Commercial channel access: established relationships with distributors, healthcare institutions, and procurement networks can create stickiness that competitors struggle to quickly replicate.
  • Portfolio selection discipline: focusing on molecules/classes where demand is durable and where competitive intensity does not compress returns excessively.
  • Partnership leverage: the capability to structure deals that align incentives—e.g., securing favorable economics, minimizing dependence on partners for core commercialization execution, or obtaining rights that support long-term monetisation.

Market positioning should also consider how AAPG competes along two axes:

  • Product positioning: differentiation by efficacy/safety, formulation, dosing convenience, or clinical guideline alignment.
  • Commercial positioning: distribution coverage, payer/institution relationships, and responsiveness to market access requirements.

From an investor standpoint, the most compelling profile is often a hybrid: credible commercialization execution paired with a pipeline/rights strategy that can refresh and extend the product base. If AAPG relies primarily on externally sourced products, the moat can be thinner—unless long-term contracts, exclusivity, or unique channels are in place.

šŸš€ Multi-Year Growth Drivers

The multi-year growth thesis for AAPG should be framed around three categories of drivers: (1) product and market expansion, (2) margin improvement, and (3) capital-efficient scaling through partnerships.

  • Geographic and channel expansion: entering additional markets, deepening penetration within existing territories, and expanding relationships with key distributors or institutional buyers. Sustainable expansion depends on regulatory readiness, supply stability, and pricing discipline.
  • Portfolio expansion and lifecycle upgrades: acquiring new product rights, expanding indication coverage, improving formulations, or adding complementary therapies to increase share of wallet within a therapeutic area.
  • Mix shift toward higher-margin products: as the portfolio matures, the revenue mix can improve if AAPG successfully scales products with favorable pricing economics, lower volatility in procurement, or stronger payer/institution acceptance.
  • Operating leverage: in pharma distribution/commercial models, fixed-cost leverage can occur as revenue grows—provided working capital is managed and returns on sales capacity remain stable.
  • Partner-enabled development: partnering can de-risk capital requirements and extend optionality. In best-case structures, AAPG can retain meaningful economics while sharing development costs and regulatory execution burden.

A high-quality long-form investor thesis should explicitly address ā€œwhat must be trueā€ for each driver. For example, geographic expansion requires that regulatory processes and supply chain logistics can scale without eroding service quality. Portfolio expansion requires that new rights are acquired at attractive economics and that clinical/regulatory timelines are achievable. Margin improvement requires either pricing power, scale benefits, or procurement advantages—not merely accounting changes.

Additionally, growth should be evaluated in light of industry cyclicality and competition. Pharma commercialization can face pricing pressure, generic substitution, and channel consolidation. AAPG’s growth durability therefore depends on whether it has a strategy that can withstand competitive pricing declines and maintain product differentiation or contractual protections.

⚠ Risk Factors to Monitor

Pharmaceutical and life-sciences groups face a distinct risk profile. An analyst-grade assessment should emphasize risk categories rather than only identify isolated negatives. For AAPG, the principal risks to monitor typically include:

  • Regulatory and compliance risk: failures in manufacturing quality systems, labeling accuracy, or regulatory submissions can delay approvals or lead to product disruptions and reputational damage.
  • Commercial execution risk: sales growth can be constrained by channel adoption, procurement cycles, reimbursement barriers, and competitor pricing tactics.
  • Dependence on partners and distribution networks: when a substantial portion of value depends on third-party commercialization, contract terms and partner performance become critical.
  • Pricing and reimbursement pressure: pricing power can erode due to formulary decisions, government procurement policies, payer behavior, and generic/biosimilar competition.
  • Working capital and liquidity risk: pharma supply chains can require inventory financing and extended receivable collection. Liquidity risk rises if sales ramp outpaces cash collection.
  • Supply chain and manufacturing risk: reliance on single or limited manufacturing sources can increase disruption risk. Quality lapses can lead to costly remediation and sales loss.
  • IP and legal risk (if applicable): disputes regarding product rights, trademarks, patents, or licensing royalties can impact future monetisation.

A key diligence practice is to ensure risk is being actively managed rather than merely disclosed. Investors should look for evidence of: (i) diversified supplier/partner relationships, (ii) robust quality systems, (iii) contract protections (exclusivity, volume floors, pricing frameworks, or termination clauses), and (iv) prudent credit management.

šŸ“Š Valuation & Market View

Valuing a pharma group like AAPG typically requires scenario-based thinking. Because pharma business models can combine recurring commercial revenue with pipeline/right-based optionality, valuation is often less about a single multiple and more about understanding the durability of cash flows and the credibility of growth pathways.

A practical market view approach generally evaluates:

  • Base business valuation: the value of current commercial operations using conservative assumptions on gross margin sustainability, operating expenses, and working capital needs.
  • Upside from portfolio expansion: incremental value from new product rights, geographic scaling, and mix improvements.
  • Optionality from development/licensing: potential upside where milestones or approvals could unlock future monetisation—discounted for execution uncertainty.

Investors should also consider valuation risk: pharma and life-sciences stocks can rerate based on shifts in perceived execution quality, regulatory confidence, partner momentum, and capital allocation discipline. AAPG’s valuation attractiveness therefore depends on the balance between (i) market expectations embedded in the current price and (ii) measurable progress on commercialization readiness and rights/portfolio strength.

Given the evergreen nature of valuation work, the most defensible method is to triangulate using multiple lenses: profitability quality (gross margin and cash conversion), balance-sheet resilience (net debt/working capital intensity, if applicable), and growth credibility (evidence that new commercial initiatives translate into repeatable demand rather than one-off channel stocking).

šŸ” Investment Takeaway

ASCENTAGE PHARMA GROUP INTERNATIONAL (AAPG) presents an investment profile typical of pharma groups where value creation depends on turning product rights, regulatory execution, and commercialization capability into durable monetisation. The central opportunity is the potential to compound value through portfolio expansion, geographic/channel growth, and margin improvement—particularly if AAPG can demonstrate resilient gross margins and disciplined working capital management.

The investment case should be approached through structured diligence: map revenue streams to their underlying economic drivers, validate the sustainability of commercialization channels and contracts, assess whether growth is repeatable and cash-generative, and confirm that regulatory and supply chain risks are being actively controlled. Where AAPG’s model includes partner-dependent monetisation or development optionality, contract terms and execution accountability become decisive.

Overall, AAPG can be viewed as a candidate for long-term consideration if the company exhibits consistent evidence of: (i) stable-to-improving unit economics, (ii) credible portfolio refresh mechanisms, and (iii) strengthened operational resilience that supports multi-year growth without disproportionate liquidity or compliance strain.


⚠ AI-generated — informational only. Validate using filings before investing.

šŸ“° Market News & Coverage

15 Stories Available

Real-time institutional reporting and market updates for AAPG.

globenewswire.com•2026-05-31

Ascentage Pharma Presents Data on Olverembatinib in CML-LBP and Ph+ BCP-ALL at ASCO 2026

ROCKVILLE, Md. and SUZHOU, China, May 31, 2026 (GLOBE NEWSWIRE) -- Ascentage Pharma Group International (NASDAQ: AAPG; HKEX: 6855), a global, commercial-stage, integrated biopharmaceutical company engaged in the discovery, development and commercialization of novel therapies to address unmet medical needs in cancer, today announced results from a Phase Ib study evaluating olverembatinib (HQP1351), the company's core product, in combination with bispecific T-cell engager antibody (immunotherapy) blinatumomab in patients with lymphoid blast phase chronic myeloid leukemia (CML-LBP) or Philadelphia chromosome-positive B-cell precursor acute lymphoblastic leukemia (Ph+ BCP-ALL) were presented in a rapid oral presentation at the 2026 American Society of Clinical Oncology (ASCO) Annual Meeting.

globenewswire.com•2026-05-31

Ascentage Pharma Presents Its First Dataset on MDM2-p53 Inhibitor Alrizomadlin (APG-115) in Pediatric Solid Tumors at ASCO 2026

ROCKVILLE, Md. and SUZHOU, China, May 31, 2026 (GLOBE NEWSWIRE) -- Ascentage Pharma Group International (NASDAQ: AAPG; HKEX: 6855), a global, commercial-stage, integrated biopharmaceutical company engaged in the discovery, development and commercialization of novel therapies to address unmet medical needs in cancer, today announced that the Company presented its first dataset of alrizomadlin (APG-115), an MDM2-p53 inhibitor from the Company's apoptosis-targeted pipeline, as monotherapy or in combination with lisaftoclax (APG-2575) in pediatric patients with relapsed/metastatic rhabdomyosarcoma (RMS) or other soft-tissue sarcomas (STSs), in a rapid oral presentation at the 62nd American Society of Clinical Oncology (ASCO) Annual Meeting.

globenewswire.com•2026-05-31

Ascentage Pharma Presents Updated Clinical Data for Olverembatinib as Second-Line Therapy in CML-CP at ASCO 2026

ROCKVILLE, Md. and SUZHOU, China, May 31, 2026 (GLOBE NEWSWIRE) -- Ascentage Pharma Group International (NASDAQ: AAPG; HKEX: 6855), a global, commercial-stage, integrated biopharmaceutical company engaged in the discovery, development and commercialization of novel, differentiated therapies to address unmet medical needs in cancer, today announced updated efficacy and safety data from a clinical study of its first approved product, olverembatinib (HQP1351), as a second-line therapy in patients with chronic-phase chronic myeloid leukemia (CML-CP) were presented in a rapid oral presentation at the 2026 American Society of Clinical Oncology (ASCO) Annual Meeting.

globenewswire.com•2026-05-31

Ascentage Pharma Presents Data on Olverembatinib in CML-LBP and Ph+ BCP-ALL at ASCO 2026

ROCKVILLE, Md. and SUZHOU, China, May 31, 2026 (GLOBE NEWSWIRE) -- Ascentage Pharma Group International (NASDAQ: AAPG; HKEX: 6855), a global, commercial-stage, integrated biopharmaceutical company engaged in the discovery, development and commercialization of novel therapies to address unmet medical needs in cancer, today announced results from a Phase Ib study evaluating olverembatinib (HQP1351), the company's core product, in combination with bispecific T-cell engager antibody (immunotherapy) blinatumomab in patients with lymphoid blast phase chronic myeloid leukemia (CML-LBP) or Philadelphia chromosome-positive B-cell precursor acute lymphoblastic leukemia (PhBCP-ALL) were presented in a rapid oral presentation at the 2026 American Society of Clinical Oncology (ASCO) Annual Meeting.

globenewswire.com•2026-05-31

Ascentage Pharma Presents Its First Dataset on MDM2-p53 Inhibitor Alrizomadlin (APG-115) in Pediatric Solid Tumors at ASCO 2026

ROCKVILLE, Md. and SUZHOU, China, May 31, 2026 (GLOBE NEWSWIRE) -- Ascentage Pharma Group International (NASDAQ: AAPG; HKEX: 6855), a global, commercial-stage, integrated biopharmaceutical company engaged in the discovery, development and commercialization of novel therapies to address unmet medical needs in cancer, today announced that the Company presented its first dataset of alrizomadlin (APG-115), an MDM2-p53 inhibitor from the Company's apoptosis-targeted pipeline, as monotherapy or in combination with lisaftoclax (APG-2575) in pediatric patients with relapsed/metastatic rhabdomyosarcoma (RMS) or other soft-tissue sarcomas (STSs), in a rapid oral presentation at the 62nd American Society of Clinical Oncology (ASCO) Annual Meeting.

globenewswire.com•2026-05-31

Ascentage Pharma Presents Updated Clinical Data for Olverembatinib as Second-Line Therapy in CML-CP at ASCO 2026

ROCKVILLE, Md. and SUZHOU, China, May 31, 2026 (GLOBE NEWSWIRE) -- Ascentage Pharma Group International (NASDAQ: AAPG; HKEX: 6855), a global, commercial-stage, integrated biopharmaceutical company engaged in the discovery, development and commercialization of novel, differentiated therapies to address unmet medical needs in cancer, today announced updated efficacy and safety data from a clinical study of its first approved product, olverembatinib (HQP1351), as a second-line therapy in patients with chronic-phase chronic myeloid leukemia (CML-CP) were presented in a rapid oral presentation at the 2026 American Society of Clinical Oncology (ASCO) Annual Meeting.

globenewswire.com•2026-05-21

Ascentage Pharma Releases Latest Clinical Data from Multiple Trials at ASCO 2026

ROCKVILLE, Md. and SUZHOU, China, May 21, 2026 (GLOBE NEWSWIRE) -- Ascentage Pharma Group International (NASDAQ: AAPG; HKEX: 6855), a global, commercial-stage, integrated biopharmaceutical company engaged in the discovery, development and commercialization of novel, differentiated therapies to address unmet medical needs in cancer, today announced that six abstracts from its clinical studies, selected for presentation at the 2026 American Society of Clinical Oncology (ASCO) Annual Meeting, are now available on ASCO's official website. Three of the six studies have been selected for rapid oral presentations, and three as poster presentation. These abstracts report data from ongoing studies evaluating the company's three lead drug candidates, including BCR-ABL inhibitor olverembatinib(HQP1351); Bcl-2 inhibitor lisaftoclax (APG-2575); and MDM2-p53 inhibitor alrizomadlin (APG-115).

globenewswire.com•2026-05-12

Ascentage Pharma to Present 17 Clinical Advances at 2026 European Hematology Association Congress

ROCKVILLE, Md. and SUZHOU, China, May 12, 2026 (GLOBE NEWSWIRE) -- Ascentage Pharma Group International (NASDAQ: AAPG; HKEX: 6855), a global, integrated biopharmaceutical company engaged in the discovery, development and commercialization of innovative therapies for cancers and other diseases, announced today that 17 clinical advances of its core assets will be featured at the 31st Congress of the European Hematology Association (EHA2026), including 8 poster presentations. The abstracts feature data from ongoing clinical studies encompassing Olverembatinib (HQP1351), China's first approved third-generation BCR-ABL inhibitor, and Lisaftoclax (APG-2575), the first approvedĀ China-developed Bcl-2 selective inhibitor. The EHA2026 Congress will convene in Stockholm, Sweden, from June 11 to 14, 2026.

globenewswire.com•2026-05-12

Ascentage Pharma to Participate in Three Upcoming Investor Conferences

ROCKVILLE, Md. and SUZHOU, China, May 12, 2026 (GLOBE NEWSWIRE) -- Ascentage Pharma Group International (NASDAQ: AAPG; HKEX: 6855) (ā€œAscentage Pharmaā€ or the ā€œCompanyā€),Ā a global, commercial stage, integrated biopharmaceutical company engaged in the discovery, development and commercialization of novel, differentiated therapies to address unmet medical needs in cancer, announced today that the Company's management is scheduled to participate in three upcoming investor conferences.

defenseworld.net•2026-04-24

Ascentage Pharma Group International – Unsponsored ADR (NASDAQ:AAPG) Receives Consensus Recommendation of ā€œBuyā€ from Analysts

Ascentage Pharma Group International - Unsponsored ADR (NASDAQ: AAPG - Get Free Report) has received an average rating of "Buy" from the seven brokerages that are presently covering the stock, Marketbeat.com reports. Five analysts have rated the stock with a buy rating and two have given a strong buy rating to the company. The average 1

globenewswire.com•2026-04-21

Ascentage Pharma to Present Data from Multiple Trials, Including Three Rapid Oral Presentations, at ASCO 2026

ROCKVILLE, Md. and SUZHOU, China, April 21, 2026 (GLOBE NEWSWIRE) -- Ascentage Pharma Group International (NASDAQ: AAPG; HKEX: 6855), a global, commercial stage, integrated biopharmaceutical company engaged in the discovery, development and commercialization of novel, differentiated therapies to address unmet medical needs in cancer, today announced that six abstracts from clinical studies of three key drug candidates have been selected for presentation at the 2026 American Society of Clinical Oncology (ASCO) Annual Meeting, to be held in person at McCormick Place in Chicago, IL, and online, May 29 – June 2, 2026. With three abstracts selected for rapid oral presentations and three abstracts selected for poster presentations, these data highlight the global innovation and clinical value of Ascentage Pharma's portfolio, inclusive of Olverembatinib (HQP1351), the first third-generation BCR-ABL inhibitor approved in China; Lisaftoclax (APG-2575), the first approved China-developed Bcl-2 selective inhibitor; and Alrizomadlin (APG-115), an MDM2-p53 inhibitor.

globenewswire.com•2026-04-21

Ascentage Pharma to Present Data from Multiple Trials, Including Three Rapid Oral Presentations, at ASCO 2026

ROCKVILLE, Md. and SUZHOU, China, April 21, 2026 (GLOBE NEWSWIRE) -- Ascentage Pharma Group International (NASDAQ: AAPG; HKEX: 6855), a global, commercial stage, integrated biopharmaceutical company engaged in the discovery, development and commercialization of novel, differentiated therapies to address unmet medical needs in cancer, today announced that six abstracts from clinical studies of three key drug candidates have been selected for presentation at the 2026 American Society of Clinical Oncology (ASCO) Annual Meeting, to be held in person at McCormick Place in Chicago, IL, and online, May 29 - June 2, 2026.

globenewswire.com•2026-04-19

Ascentage Pharma to Present Four Promising Preclinical Studies Demonstrating the Potential of Combination Therapies at American Association for Cancer Research (AACR) 2026 Annual Meeting

ROCKVILLE, Md. and SUZHOU, China, April 19, 2026 (GLOBE NEWSWIRE) -- Ascentage Pharma Group International (NASDAQ: AAPG; HKEX: 6855), a global, commercial stage, integrated biopharmaceutical company engaged in the discovery, development and commercialization of novel, differentiated therapies to address unmet medical needs in cancer, announced that it will present four preclinical studies in poster format at the American Association for Cancer Research (AACR) 2026 Annual Meeting, held April 17 to 22, 2026 in San Diego, CA, USA.

globenewswire.com•2026-04-19

Ascentage Pharma to Present Four Promising Preclinical Studies Demonstrating the Potential of Combination Therapies at American Association for Cancer Research (AACR) 2026 Annual Meeting

ROCKVILLE, Md. and SUZHOU, China, April 19, 2026 (GLOBE NEWSWIRE) -- Ascentage Pharma Group International (NASDAQ: AAPG; HKEX: 6855), a global, commercial stage, integrated biopharmaceutical company engaged in the discovery, development and commercialization of novel, differentiated therapies to address unmet medical needs in cancer, announced that it will present four preclinical studies in poster format at the American Association for Cancer Research (AACR) 2026 Annual Meeting, held April 17 to 22, 2026 in San Diego, CA, USA.

defenseworld.net•2026-04-14

Ascentage Pharma Group International – Unsponsored ADR (NASDAQ:AAPG) Short Interest Update

Ascentage Pharma Group International - Unsponsored ADR (NASDAQ: AAPG - Get Free Report) was the recipient of a significant increase in short interest in March. As of March 31st, there was short interest totaling 1,470 shares, an increase of 54.6% from the March 15th total of 951 shares. Based on an average daily trading volume, of

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šŸ“‹ Official Regulatory 10-K / 10-Q SEC Filings

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Ā© 2026 Stock Market Info — ASCENTAGE PHARMA GROUP INTERNATIONAL (AAPG) Financial Profile