AAPL337.90+0.99 (+0.29%) ▲|ABBV266.37+9.46 (+3.68%) ▲|ABT109.22+4.73 (+4.53%) ▲|ACN165.68+11.62 (+7.54%) ▲|ADBE250.65+12.90 (+5.42%) ▲|AMAT471.63-45.26 (-8.76%) ▼|AMD447.58-47.37 (-9.57%) ▼|AMGN397.10+20.84 (+5.54%) ▲|AMT176.66+9.92 (+5.95%) ▲|AMZN229.83-1.56 (-0.67%) ▼|AVGO375.73-7.49 (-1.95%) ▼|AXP335.38-0.01 (0.00%) ▼|BA221.24+9.74 (+4.61%) ▲|BAC62.30+0.17 (+0.27%) ▲|BKNG195.24+8.45 (+4.52%) ▲|BLK1,081.76+19.62 (+1.85%) ▲|BMY64.82+2.26 (+3.61%) ▲|BNY155.84-1.94 (-1.23%) ▼|BRK-B510.65+13.47 (+2.71%) ▲|C131.91-1.19 (-0.89%) ▼|CAT827.31-45.97 (-5.26%) ▼|CL94.85+2.87 (+3.12%) ▲|CMCSA23.83+1.03 (+4.50%) ▲|COF208.47+1.42 (+0.69%) ▲|COP116.75+1.17 (+1.01%) ▲|COST984.80+33.22 (+3.49%) ▲|CRM181.37+7.77 (+4.47%) ▲|CSCO114.01-0.56 (-0.49%) ▼|CVS108.70+1.63 (+1.52%) ▲|CVX191.05+1.05 (+0.55%) ▲|DE636.17+11.15 (+1.78%) ▲|DHR203.77+7.27 (+3.70%) ▲|DIS98.87+2.22 (+2.30%) ▲|DUK132.33+3.50 (+2.72%) ▲|EMR150.88+1.58 (+1.06%) ▲|FDX309.64-1.15 (-0.37%) ▼|GD392.59+3.45 (+0.89%) ▲|GE364.02+2.41 (+0.67%) ▲|GEV918.83-77.74 (-7.80%) ▼|GILD135.29+4.77 (+3.65%) ▲|GM88.94+1.90 (+2.18%) ▲|GOOG327.45+0.88 (+0.27%) ▲|GOOGL327.60+1.04 (+0.32%) ▲|GS1,025.39-22.84 (-2.18%) ▼|HD346.74+10.65 (+3.17%) ▲|HON249.21+3.46 (+1.41%) ▲|IBM217.42+1.14 (+0.52%) ▲|INTC83.93-7.74 (-8.44%) ▼|INTU319.89+15.98 (+5.26%) ▲|ISRG370.77+13.94 (+3.91%) ▲|JNJ272.84+6.89 (+2.59%) ▲|JPM356.28+0.08 (+0.02%) ▲|KO89.84+5.77 (+6.86%) ▲|LIN520.82+13.80 (+2.72%) ▲|LLY1,226.52+28.99 (+2.42%) ▲|LMT587.06+7.06 (+1.22%) ▲|LOW219.39+7.84 (+3.71%) ▲|LRCX261.45-30.16 (-10.34%) ▼|MA561.16+9.45 (+1.71%) ▲|MCD278.58+7.91 (+2.92%) ▲|MDLZ63.31+2.64 (+4.35%) ▲|MDT88.80+4.58 (+5.43%) ▲|META593.99+0.12 (+0.02%) ▲|MMM182.68+4.45 (+2.50%) ▲|MO76.78+3.89 (+5.34%) ▲|MRK134.86+4.10 (+3.14%) ▲|MS209.60-4.96 (-2.31%) ▼|MSFT395.76+6.66 (+1.71%) ▲|MU801.74-98.47 (-10.94%) ▼|NEE90.81+1.98 (+2.23%) ▲|NFLX73.52+3.12 (+4.43%) ▲|NKE43.09+0.95 (+2.24%) ▲|NOW109.84+4.28 (+4.05%) ▲|NVDA193.84-2.67 (-1.36%) ▼|ORCL115.26-4.64 (-3.87%) ▼|PEP144.80+5.01 (+3.58%) ▲|PFE25.43+0.76 (+3.06%) ▲|PG152.57+3.94 (+2.65%) ▲|PLTR119.12-12.41 (-9.44%) ▼|PM206.49+10.83 (+5.54%) ▲|QCOM166.35-3.69 (-2.17%) ▼|RTX220.86+2.44 (+1.12%) ▲|SBUX105.09+1.44 (+1.39%) ▲|SCHW105.56+1.38 (+1.32%) ▲|SO98.55+2.07 (+2.15%) ▲|SPG236.89+5.22 (+2.25%) ▲|T25.14+0.72 (+2.93%) ▲|TMO580.32+20.79 (+3.72%) ▲|TMUS185.30+8.09 (+4.56%) ▲|TSLA302.13-7.09 (-2.29%) ▼|TXN277.03-2.39 (-0.85%) ▼|UBER69.25+1.07 (+1.57%) ▲|UNH418.36+0.72 (+0.17%) ▲|UNP301.69+2.39 (+0.80%) ▲|UPS107.62-5.33 (-4.72%) ▼|USB63.91+0.42 (+0.66%) ▲|V365.17+2.64 (+0.73%) ▲|VZ48.70+1.38 (+2.91%) ▲|WFC87.20-0.07 (-0.08%) ▼|WMT115.48+3.74 (+3.35%) ▲|XOM156.00+1.23 (+0.79%) ▲|AAPL337.90+0.99 (+0.29%) ▲|ABBV266.37+9.46 (+3.68%) ▲|ABT109.22+4.73 (+4.53%) ▲|ACN165.68+11.62 (+7.54%) ▲|ADBE250.65+12.90 (+5.42%) ▲|AMAT471.63-45.26 (-8.76%) ▼|AMD447.58-47.37 (-9.57%) ▼|AMGN397.10+20.84 (+5.54%) ▲|AMT176.66+9.92 (+5.95%) ▲|AMZN229.83-1.56 (-0.67%) ▼|AVGO375.73-7.49 (-1.95%) ▼|AXP335.38-0.01 (0.00%) ▼|BA221.24+9.74 (+4.61%) ▲|BAC62.30+0.17 (+0.27%) ▲|BKNG195.24+8.45 (+4.52%) ▲|BLK1,081.76+19.62 (+1.85%) ▲|BMY64.82+2.26 (+3.61%) ▲|BNY155.84-1.94 (-1.23%) ▼|BRK-B510.65+13.47 (+2.71%) ▲|C131.91-1.19 (-0.89%) ▼|CAT827.31-45.97 (-5.26%) ▼|CL94.85+2.87 (+3.12%) ▲|CMCSA23.83+1.03 (+4.50%) ▲|COF208.47+1.42 (+0.69%) ▲|COP116.75+1.17 (+1.01%) ▲|COST984.80+33.22 (+3.49%) ▲|CRM181.37+7.77 (+4.47%) ▲|CSCO114.01-0.56 (-0.49%) ▼|CVS108.70+1.63 (+1.52%) ▲|CVX191.05+1.05 (+0.55%) ▲|DE636.17+11.15 (+1.78%) ▲|DHR203.77+7.27 (+3.70%) ▲|DIS98.87+2.22 (+2.30%) ▲|DUK132.33+3.50 (+2.72%) ▲|EMR150.88+1.58 (+1.06%) ▲|FDX309.64-1.15 (-0.37%) ▼|GD392.59+3.45 (+0.89%) ▲|GE364.02+2.41 (+0.67%) ▲|GEV918.83-77.74 (-7.80%) ▼|GILD135.29+4.77 (+3.65%) ▲|GM88.94+1.90 (+2.18%) ▲|GOOG327.45+0.88 (+0.27%) ▲|GOOGL327.60+1.04 (+0.32%) ▲|GS1,025.39-22.84 (-2.18%) ▼|HD346.74+10.65 (+3.17%) ▲|HON249.21+3.46 (+1.41%) ▲|IBM217.42+1.14 (+0.52%) ▲|INTC83.93-7.74 (-8.44%) ▼|INTU319.89+15.98 (+5.26%) ▲|ISRG370.77+13.94 (+3.91%) ▲|JNJ272.84+6.89 (+2.59%) ▲|JPM356.28+0.08 (+0.02%) ▲|KO89.84+5.77 (+6.86%) ▲|LIN520.82+13.80 (+2.72%) ▲|LLY1,226.52+28.99 (+2.42%) ▲|LMT587.06+7.06 (+1.22%) ▲|LOW219.39+7.84 (+3.71%) ▲|LRCX261.45-30.16 (-10.34%) ▼|MA561.16+9.45 (+1.71%) ▲|MCD278.58+7.91 (+2.92%) ▲|MDLZ63.31+2.64 (+4.35%) ▲|MDT88.80+4.58 (+5.43%) ▲|META593.99+0.12 (+0.02%) ▲|MMM182.68+4.45 (+2.50%) ▲|MO76.78+3.89 (+5.34%) ▲|MRK134.86+4.10 (+3.14%) ▲|MS209.60-4.96 (-2.31%) ▼|MSFT395.76+6.66 (+1.71%) ▲|MU801.74-98.47 (-10.94%) ▼|NEE90.81+1.98 (+2.23%) ▲|NFLX73.52+3.12 (+4.43%) ▲|NKE43.09+0.95 (+2.24%) ▲|NOW109.84+4.28 (+4.05%) ▲|NVDA193.84-2.67 (-1.36%) ▼|ORCL115.26-4.64 (-3.87%) ▼|PEP144.80+5.01 (+3.58%) ▲|PFE25.43+0.76 (+3.06%) ▲|PG152.57+3.94 (+2.65%) ▲|PLTR119.12-12.41 (-9.44%) ▼|PM206.49+10.83 (+5.54%) ▲|QCOM166.35-3.69 (-2.17%) ▼|RTX220.86+2.44 (+1.12%) ▲|SBUX105.09+1.44 (+1.39%) ▲|SCHW105.56+1.38 (+1.32%) ▲|SO98.55+2.07 (+2.15%) ▲|SPG236.89+5.22 (+2.25%) ▲|T25.14+0.72 (+2.93%) ▲|TMO580.32+20.79 (+3.72%) ▲|TMUS185.30+8.09 (+4.56%) ▲|TSLA302.13-7.09 (-2.29%) ▼|TXN277.03-2.39 (-0.85%) ▼|UBER69.25+1.07 (+1.57%) ▲|UNH418.36+0.72 (+0.17%) ▲|UNP301.69+2.39 (+0.80%) ▲|UPS107.62-5.33 (-4.72%) ▼|USB63.91+0.42 (+0.66%) ▲|V365.17+2.64 (+0.73%) ▲|VZ48.70+1.38 (+2.91%) ▲|WFC87.20-0.07 (-0.08%) ▼|WMT115.48+3.74 (+3.35%) ▲|XOM156.00+1.23 (+0.79%) ▲|
26.3 C
New York
Tuesday, July 28, 2026

Tag: inhibitors

Outlook Therapeutics Announces LYTENAVA™ FDA Approval as the First and Only FDA-Approved Ophthalmic Bevacizumab for the Treatment of Wet AMD

Landmark FDA Approval Is an Important Milestone in Retina Care, Bringing Patients and Physicians an Ophthalmic Bevacizumab Developed Specifically for the Eye Following Years of Rigorous Clinical and Regulatory Evaluation

Johnson & Johnson presents new IMAAVY®▼ (nipocalimab) data at European Academy of Neurology (EAN) 2026 Congress reinforcing sustained disease control in generalised myasthenia gravis

BEERSE, BELGIUM, June 26, 2026 (GLOBE NEWSWIRE) -- Johnson & Johnson today announced new data across 12 abstracts at the European Academy of Neurology (EAN) 2026 Congress that offer additional insight into the use of IMAAVY®▼(nipocalimab) throughout clinically relevant points in the generalised myasthenia gravis (gMG) treatment journey. The analyses include adults with anti-AChRa or anti-MuSKb antibody-positive gMG who were early in their disease course or had lower baseline symptom burden – providing insight into the potential importance of addressing pathogenic immunoglobulin G (IgG) early in disease progression where use of advanced therapies may be less common.1,2 Additional research to be shared include outcomes shortly after common infections, which are a known cause of disease exacerbations in gMG, and plans to address evidence gaps in the use of nipocalimab during pregnancy.3,4

Johnson & Johnson presents new IMAAVY® (nipocalimab-aahu) data at European Academy of Neurology (EAN) 2026 Congress reinforcing sustained disease control in generalized myasthenia gravis

New analyses from the Phase 3 Vivacity-MG3 study support the impact of IMAAVY in anti-AChR+a, anti-MuSK+b adult patients with generalized myasthenia gravis (gMG) including...

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...

Complex Small Molecules Are Changing Drug R&D

WuXi AppTec details how structural complexity in protein degraders, covalent agents, and kinase programs is reshaping what integrated CRDMOs must deliver.

Everest Medicines Announces China NMPA Acceptance of the Biologics License Application for LEROCHOL® in Adults with Hypercholesterolemia

SHANGHAI, June 26, 2026 /PRNewswire/ -- Everest Medicines (HKEX 1952.HK, "Everest", or the "Company"), a biopharmaceutical company focused on the discovery, clinical development, manufacturing...

JellyFil Discloses 2026 Botanical Ingredient Sourcing, cGMP Manufacturing Standards, Caffeine Content, and Consumer Safety Considerations for Its Premium Gummy Dietary Supplement

JellyFil discloses 2026 gummy supplement ingredient origins, cGMP manufacturing standards, caffeine content, and drug interaction guidance.

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 —

Sagimet Biosciences Announces Participation in Upcoming Investor Conference and Inducement Grant Under Nasdaq Listing Rule 5635(c)(4)

SAN MATEO, Calif., June 22, 2026 (GLOBE NEWSWIRE) -- Sagimet Biosciences Inc. (Nasdaq: SGMT), a clinical-stage biopharmaceutical company developing novel therapeutics targeting dysfunctional metabolic and fibrotic pathways, today announced that management will participate in 1x1 investor meetings at the Leerink Partners Therapeutics Forum in Boston, MA on July 15, 2026.

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...

Nura Bio Completes $73.8M Series B Financing and Advances Pipeline of SARM1 Inhibitors

Nura Bio announced the completion of a Series B financing and the advancement of its two clinical-stage SARM1 inhibitor programs

Innovative Molecules Expands Virology Pipeline with Novel EBV Antiviral Program

MUNICH, June 16, 2026 /PRNewswire/ -- Innovative Molecules GmbH ("IM"), a clinical-stage biopharmaceutical company focused on herpesvirus-mediated diseases, today announced the advancement of its virology...

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.

Crinetics Presents Long Term Data at ENDO 2026 Confirming PALSONIFY™ (paltusotine) Provides Durable, Consistent Acromegaly Control

Data from up to two years of treatment in PATHFNDR-1 and PATHFNDR-2 open-label extension studies show PALSONIFY maintained lower IGF-1 levels and stable symptoms

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