AAPL327.44-6.30 (-1.89%) ▼|ABBV254.00-0.49 (-0.19%) ▼|ABT101.20+0.52 (+0.51%) ▲|ACN141.65-1.92 (-1.34%) ▼|ADBE228.72-8.53 (-3.60%) ▼|AMAT538.27+8.61 (+1.63%) ▲|AMD511.80+16.04 (+3.23%) ▲|AMGN366.92+0.63 (+0.17%) ▲|AMT168.89-1.17 (-0.69%) ▼|AMZN249.62+2.39 (+0.97%) ▲|AVGO378.57+7.75 (+2.09%) ▲|AXP353.16-2.20 (-0.62%) ▼|BA209.73-4.30 (-2.01%) ▼|BAC60.71-0.56 (-0.91%) ▼|BKNG179.14-2.54 (-1.40%) ▼|BLK1,057.21-14.99 (-1.40%) ▼|BMY61.25+0.51 (+0.84%) ▲|BNY157.78+0.65 (+0.41%) ▲|BRK-B490.83-0.08 (-0.02%) ▼|C129.51+0.15 (+0.12%) ▲|CAT879.13+0.48 (+0.05%) ▲|CL91.73-0.72 (-0.78%) ▼|CMCSA23.64-0.16 (-0.65%) ▼|COF207.61-0.42 (-0.20%) ▼|COP115.18+0.47 (+0.41%) ▲|COST944.73+3.86 (+0.41%) ▲|CRM168.87-1.90 (-1.11%) ▼|CSCO112.52+0.58 (+0.52%) ▲|CVS108.01+0.54 (+0.50%) ▲|CVX188.51+1.13 (+0.60%) ▲|DE591.17-6.07 (-1.02%) ▼|DHR203.49-0.34 (-0.17%) ▼|DIS96.40-1.27 (-1.30%) ▼|DUK126.68+1.67 (+1.34%) ▲|EMR137.09-2.45 (-1.76%) ▼|FDX308.61-4.38 (-1.40%) ▼|GD371.98+3.40 (+0.92%) ▲|GE347.96-0.87 (-0.25%) ▼|GEV1,081.24+23.40 (+2.21%) ▲|GILD133.87-0.41 (-0.31%) ▼|GM76.01-0.06 (-0.08%) ▼|GOOG358.50+12.38 (+3.58%) ▲|GOOGL358.73+11.96 (+3.45%) ▲|GS1,060.00-5.22 (-0.49%) ▼|HD335.22-3.65 (-1.08%) ▼|HON225.17+0.15 (+0.07%) ▲|IBM210.51-2.17 (-1.02%) ▼|INTC97.78+2.74 (+2.88%) ▲|INTU282.98-8.12 (-2.79%) ▼|ISRG346.67+1.25 (+0.36%) ▲|JNJ251.70-1.34 (-0.53%) ▼|JPM341.29+0.19 (+0.06%) ▲|KO82.17+0.61 (+0.75%) ▲|LIN515.25+2.03 (+0.40%) ▲|LLY1,169.32-9.79 (-0.83%) ▼|LMT511.67+2.90 (+0.57%) ▲|LOW204.39-4.35 (-2.08%) ▼|LRCX312.98-0.33 (-0.10%) ▼|MA542.86-0.75 (-0.14%) ▼|MCD268.87+1.16 (+0.43%) ▲|MDLZ60.29-0.71 (-1.16%) ▼|MDT83.32+0.12 (+0.14%) ▲|META643.84-2.17 (-0.34%) ▼|MMM161.29+1.45 (+0.91%) ▲|MO74.58+0.37 (+0.50%) ▲|MRK126.61-0.89 (-0.70%) ▼|MS213.84-1.67 (-0.77%) ▼|MSFT394.25+0.43 (+0.11%) ▲|MU872.51+23.56 (+2.77%) ▲|NEE89.30+0.50 (+0.56%) ▲|NFLX67.54-1.41 (-2.05%) ▼|NKE43.12-0.64 (-1.46%) ▼|NOW99.07-4.17 (-4.04%) ▼|NVDA205.22+2.41 (+1.19%) ▲|ORCL120.58-5.83 (-4.61%) ▼|PEP136.64-0.49 (-0.35%) ▼|PFE24.94-0.12 (-0.46%) ▼|PG149.62-0.36 (-0.24%) ▼|PLTR132.80+0.42 (+0.32%) ▲|PM193.05+0.07 (+0.04%) ▲|QCOM171.76-0.02 (-0.01%) ▼|RTX196.71+3.20 (+1.65%) ▲|SBUX106.09+0.60 (+0.57%) ▲|SCHW100.49-1.07 (-1.05%) ▼|SO95.43+0.13 (+0.14%) ▲|SPG230.04+1.34 (+0.59%) ▲|T21.83+0.02 (+0.09%) ▲|TMO529.02-3.47 (-0.65%) ▼|TMUS193.04+0.61 (+0.32%) ▲|TSLA374.72-6.13 (-1.61%) ▼|TXN289.55+5.53 (+1.95%) ▲|UBER72.23-0.23 (-0.32%) ▼|UNH422.09-4.00 (-0.94%) ▼|UNP300.40-1.35 (-0.45%) ▼|UPS113.72-4.00 (-3.40%) ▼|USB63.27+0.13 (+0.21%) ▲|V359.07+0.51 (+0.14%) ▲|VZ43.48-0.12 (-0.26%) ▼|WFC86.96-0.55 (-0.63%) ▼|WMT113.99-0.25 (-0.22%) ▼|XOM148.37+1.01 (+0.68%) ▲|AAPL327.44-6.30 (-1.89%) ▼|ABBV254.00-0.49 (-0.19%) ▼|ABT101.20+0.52 (+0.51%) ▲|ACN141.65-1.92 (-1.34%) ▼|ADBE228.72-8.53 (-3.60%) ▼|AMAT538.27+8.61 (+1.63%) ▲|AMD511.80+16.04 (+3.23%) ▲|AMGN366.92+0.63 (+0.17%) ▲|AMT168.89-1.17 (-0.69%) ▼|AMZN249.62+2.39 (+0.97%) ▲|AVGO378.57+7.75 (+2.09%) ▲|AXP353.16-2.20 (-0.62%) ▼|BA209.73-4.30 (-2.01%) ▼|BAC60.71-0.56 (-0.91%) ▼|BKNG179.14-2.54 (-1.40%) ▼|BLK1,057.21-14.99 (-1.40%) ▼|BMY61.25+0.51 (+0.84%) ▲|BNY157.78+0.65 (+0.41%) ▲|BRK-B490.83-0.08 (-0.02%) ▼|C129.51+0.15 (+0.12%) ▲|CAT879.13+0.48 (+0.05%) ▲|CL91.73-0.72 (-0.78%) ▼|CMCSA23.64-0.16 (-0.65%) ▼|COF207.61-0.42 (-0.20%) ▼|COP115.18+0.47 (+0.41%) ▲|COST944.73+3.86 (+0.41%) ▲|CRM168.87-1.90 (-1.11%) ▼|CSCO112.52+0.58 (+0.52%) ▲|CVS108.01+0.54 (+0.50%) ▲|CVX188.51+1.13 (+0.60%) ▲|DE591.17-6.07 (-1.02%) ▼|DHR203.49-0.34 (-0.17%) ▼|DIS96.40-1.27 (-1.30%) ▼|DUK126.68+1.67 (+1.34%) ▲|EMR137.09-2.45 (-1.76%) ▼|FDX308.61-4.38 (-1.40%) ▼|GD371.98+3.40 (+0.92%) ▲|GE347.96-0.87 (-0.25%) ▼|GEV1,081.24+23.40 (+2.21%) ▲|GILD133.87-0.41 (-0.31%) ▼|GM76.01-0.06 (-0.08%) ▼|GOOG358.50+12.38 (+3.58%) ▲|GOOGL358.73+11.96 (+3.45%) ▲|GS1,060.00-5.22 (-0.49%) ▼|HD335.22-3.65 (-1.08%) ▼|HON225.17+0.15 (+0.07%) ▲|IBM210.51-2.17 (-1.02%) ▼|INTC97.78+2.74 (+2.88%) ▲|INTU282.98-8.12 (-2.79%) ▼|ISRG346.67+1.25 (+0.36%) ▲|JNJ251.70-1.34 (-0.53%) ▼|JPM341.29+0.19 (+0.06%) ▲|KO82.17+0.61 (+0.75%) ▲|LIN515.25+2.03 (+0.40%) ▲|LLY1,169.32-9.79 (-0.83%) ▼|LMT511.67+2.90 (+0.57%) ▲|LOW204.39-4.35 (-2.08%) ▼|LRCX312.98-0.33 (-0.10%) ▼|MA542.86-0.75 (-0.14%) ▼|MCD268.87+1.16 (+0.43%) ▲|MDLZ60.29-0.71 (-1.16%) ▼|MDT83.32+0.12 (+0.14%) ▲|META643.84-2.17 (-0.34%) ▼|MMM161.29+1.45 (+0.91%) ▲|MO74.58+0.37 (+0.50%) ▲|MRK126.61-0.89 (-0.70%) ▼|MS213.84-1.67 (-0.77%) ▼|MSFT394.25+0.43 (+0.11%) ▲|MU872.51+23.56 (+2.77%) ▲|NEE89.30+0.50 (+0.56%) ▲|NFLX67.54-1.41 (-2.05%) ▼|NKE43.12-0.64 (-1.46%) ▼|NOW99.07-4.17 (-4.04%) ▼|NVDA205.22+2.41 (+1.19%) ▲|ORCL120.58-5.83 (-4.61%) ▼|PEP136.64-0.49 (-0.35%) ▼|PFE24.94-0.12 (-0.46%) ▼|PG149.62-0.36 (-0.24%) ▼|PLTR132.80+0.42 (+0.32%) ▲|PM193.05+0.07 (+0.04%) ▲|QCOM171.76-0.02 (-0.01%) ▼|RTX196.71+3.20 (+1.65%) ▲|SBUX106.09+0.60 (+0.57%) ▲|SCHW100.49-1.07 (-1.05%) ▼|SO95.43+0.13 (+0.14%) ▲|SPG230.04+1.34 (+0.59%) ▲|T21.83+0.02 (+0.09%) ▲|TMO529.02-3.47 (-0.65%) ▼|TMUS193.04+0.61 (+0.32%) ▲|TSLA374.72-6.13 (-1.61%) ▼|TXN289.55+5.53 (+1.95%) ▲|UBER72.23-0.23 (-0.32%) ▼|UNH422.09-4.00 (-0.94%) ▼|UNP300.40-1.35 (-0.45%) ▼|UPS113.72-4.00 (-3.40%) ▼|USB63.27+0.13 (+0.21%) ▲|V359.07+0.51 (+0.14%) ▲|VZ43.48-0.12 (-0.26%) ▼|WFC86.96-0.55 (-0.63%) ▼|WMT113.99-0.25 (-0.22%) ▼|XOM148.37+1.01 (+0.68%) ▲|
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Monday, July 20, 2026

Tag: systemic therapy

Castle Biosciences Announces New York State Department of Health Approval of its AdvanceAD-Tx™ Test

Approval expands access to Castle's precision medicine test designed to guide systemic treatment decision making in patients with moderate-to-severe atopic dermatitisFRIENDSWOOD, Texas, July 14,...

SKYRIZI® (risankizumab-rzaa) Now FDA Approved for Pediatric Use in Psoriatic Disease

SKYRIZI (risankizumab-rzaa) is now approved for patients six years of age and older with moderate-to-severe plaque psoriasis or active psoriatic arthritis Approval includes a...

Lilly’s Jaypirca (pirtobrutinib) recommended by CHMP for approval in the European Union for adults with chronic lymphocytic leukemia (CLL) across all lines of therapy

The positive opinion is based on results from the Phase 3 BRUIN CLL-313 and BRUIN CLL-314 trials, previously presented at the 2025 American Society...

HUTCHMED Highlights Pivotal Phase II Data for Fanregratinib in Intrahepatic Cholangiocarcinoma Presented at ESMO Gastrointestinal Cancers Congress 2026

— Registration-enabling study demonstrated high clinically meaningful objective responses, achieving rapid and durable disease control —

AbbVie Announces European Commission Approval of SKYRIZI® (risankizumab) for the Treatment of Pediatric Patients with Moderate to Severe Plaque Psoriasis

SKYRIZI® (risankizumab) expands its indication for children and adolescents six years of age and older with moderate to severe plaque psoriasis1Approval was based on...

Karmanos Cancer Institute Reaches Historic Growth Milestone, Positioning Itself as a Leader in Oncology Care Delivery

Unprecedented patient demand reflects a deliberate strategy focused on access, advanced therapies and integrated researchDETROIT, June 22, 2026 /PRNewswire/ -- The Barbara Ann Karmanos Cancer...

Ascentage Pharma Presents Multiple Clinical Updates at EHA2026 Congress

ROCKVILLE, Md. and SUZHOU, China, June 14, 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, announced today that seventeen clinical updates from its core assets were presented at the 31st Congress of the European Hematology Association (EHA2026), including eight poster presentations. The presentations featured data from ongoing clinical studies of olverembatinib (HQP1351), the first third-generation BCR-ABL1 inhibitor approved in China, and lisaftoclax (APG-2575), the first approved China-developed Bcl-2 selective inhibitor. The EHA2026 Congress convened in Stockholm, Sweden, from June 11 to 14, 2026.

Lilly’s Jaypirca (pirtobrutinib) significantly reduced the risk of disease progression or death by 45% when added to a venetoclax time-limited regimen in people with...

BRUIN CLL-322 is the first Phase 3 study to demonstrate superiority over a venetoclax-containing control arm in CLL, and, with the majority of patients...

World’s First CLDN18.2 ADC for Regulatory Review: Innovent Biologics Announces IBI343 (arcotatug tavatecan) Met Primary Endpoint in International Phase 3 Study in Advanced Refractory...

SAN FRANCISCO and SUZHOU, China, June 4, 2026 /PRNewswire/ -- Innovent Biologics, Inc. ("Innovent") (HKEX: 01801), a world-class biopharmaceutical company that develops, manufactures and...

2026 ASCO LBA | Juncell Therapeutics’ GC101 TIL Therapy Achieves Primary Endpoint in the Pivotal Phase II Trial for PD-1 Antibody Failed Advanced Melanoma

SHANGHAI, June 3, 2026 /PRNewswire/ -- On June 1 (Chicago time), in a Late-Breaking Abstract (LBA) oral presentation at the 2026 American Society of Clinical...

Ascentage Pharma Announces Global Registrational Phase III Study of Lisaftoclax for First-line Treatment of Patients with Higher-Risk Myelodysplastic Syndrome Cleared by US FDA and...

ROCKVILLE, Md. and SUZHOU, China, Aug. 17, 2025 (GLOBE NEWSWIRE) -- Ascentage Pharma (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 has received clearance by the U.S. Food and Drug Administration (FDA) and the European Medicines Agency (EMA) to conduct GLORA-4 study (NCT06641414), a global registrational Phase III study of lisaftoclax (APG-2575), a proprietary Bcl-2 inhibitor, in combination with azacitidine (AZA), for the treatment of patients with newly diagnosed higher-risk myelodysplastic syndrome (HR-MDS).

TYK2 Inhibitors Market to Drive Enormous Growth by 2034 Due to Strong Pipeline and Expanding Indications | DelveInsight

The TYK2 inhibitor market is expected to witness substantial growth in the coming years, driven by the increasing prevalence of autoimmune diseases, robust clinical...

ADC Therapeutics Makes Grants to New Employees Under Inducement Plan

LAUSANNE, Switzerland, Aug. 1, 2025 /PRNewswire/ -- ADC Therapeutics SA (NYSE: ADCT), a commercial-stage global leader and pioneer in the field of antibody drug...

Cabometyx® approved in the EU for previously treated advanced neuroendocrine tumors

PARIS, FRANCE, 24 July 2025 - Ipsen announced today that the European Commission has approved Cabometyx® (cabozantinib) for adult patients with unresectable or metastatic, well differentiated pancreatic (pNET) and extra-pancreatic (epNET) neuroendocrine tumors who have progressed following at least one prior systemic therapy other than somatostatin analogues.

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