AAPL341.32+1.24 (+0.36%) ▲|ABBV266.20+3.00 (+1.14%) ▲|ABT109.56+2.29 (+2.13%) ▲|ACN171.48+6.82 (+4.14%) ▲|ADBE258.88+9.70 (+3.89%) ▲|AMAT451.28-25.18 (-5.28%) ▼|AMD432.93-21.69 (-4.77%) ▼|AMGN395.09+1.99 (+0.51%) ▲|AMT175.97+4.47 (+2.61%) ▲|AMZN227.71-3.15 (-1.36%) ▼|AVGO375.10-5.82 (-1.53%) ▼|AXP333.82-2.81 (-0.83%) ▼|BA212.31-9.26 (-4.18%) ▼|BAC61.89-0.74 (-1.17%) ▼|BKNG200.00+0.69 (+0.35%) ▲|BLK1,101.76+4.21 (+0.38%) ▲|BMY63.65+0.05 (+0.08%) ▲|BNY154.89-1.60 (-1.02%) ▼|BRK-B510.00-2.37 (-0.46%) ▼|C128.77-3.70 (-2.79%) ▼|CAT803.28-37.57 (-4.47%) ▼|CL92.19-0.54 (-0.58%) ▼|CMCSA24.44+0.25 (+1.03%) ▲|COF211.67-0.74 (-0.35%) ▼|COP118.37+4.27 (+3.74%) ▲|COST973.24+6.66 (+0.69%) ▲|CRM183.83+2.33 (+1.28%) ▲|CSCO116.35+0.77 (+0.66%) ▲|CVS108.31-1.03 (-0.94%) ▼|CVX192.55+4.97 (+2.65%) ▲|DE620.23-19.62 (-3.07%) ▼|DHR201.84+2.79 (+1.40%) ▲|DIS98.92+0.03 (+0.03%) ▲|DUK130.08+0.84 (+0.65%) ▲|EMR148.48-3.33 (-2.19%) ▼|FDX310.13-2.51 (-0.80%) ▼|GD393.38+0.19 (+0.05%) ▲|GE356.32-7.28 (-2.00%) ▼|GEV923.17-20.21 (-2.14%) ▼|GILD133.38-0.94 (-0.70%) ▼|GM91.00+0.70 (+0.77%) ▲|GOOG331.19-1.41 (-0.42%) ▼|GOOGL332.34-1.37 (-0.41%) ▼|GS990.92-42.42 (-4.11%) ▼|HD338.33-6.14 (-1.78%) ▼|HON242.76-4.30 (-1.74%) ▼|IBM227.34-0.22 (-0.09%) ▼|INTC83.85-2.45 (-2.84%) ▼|INTU326.39+13.40 (+4.28%) ▲|ISRG356.63-5.17 (-1.43%) ▼|JNJ268.16+1.43 (+0.54%) ▲|JPM350.20-7.12 (-1.99%) ▼|KO90.72+2.45 (+2.78%) ▲|LIN509.84-1.34 (-0.26%) ▼|LLY1,223.45+2.79 (+0.23%) ▲|LMT578.65-2.66 (-0.46%) ▼|LOW216.07-2.18 (-1.00%) ▼|LRCX258.03-11.58 (-4.30%) ▼|MA564.48+1.73 (+0.31%) ▲|MCD271.71-1.31 (-0.48%) ▼|MDLZ65.59+3.11 (+4.98%) ▲|MDT87.80+0.92 (+1.06%) ▲|META586.87-6.54 (-1.10%) ▼|MMM181.61-0.88 (-0.48%) ▼|MO75.43+0.61 (+0.82%) ▲|MRK130.75-1.07 (-0.81%) ▼|MS205.87-5.71 (-2.70%) ▼|MSFT392.47-0.89 (-0.23%) ▼|MU788.34-32.19 (-3.92%) ▼|NEE89.79+0.51 (+0.57%) ▲|NFLX72.02-0.38 (-0.52%) ▼|NKE42.55-0.50 (-1.16%) ▼|NOW113.16+2.54 (+2.30%) ▲|NVDA191.44-5.57 (-2.83%) ▼|ORCL117.86-2.10 (-1.75%) ▼|PEP145.02+2.16 (+1.51%) ▲|PFE25.22-0.03 (-0.12%) ▼|PG145.28-3.61 (-2.42%) ▼|PLTR123.59+0.06 (+0.05%) ▲|PM201.15+0.98 (+0.49%) ▲|QCOM159.03-3.85 (-2.36%) ▼|RTX217.66-0.92 (-0.42%) ▼|SBUX103.59+0.49 (+0.48%) ▲|SCHW105.77-0.20 (-0.19%) ▼|SO97.13+0.35 (+0.36%) ▲|SPG237.22+0.52 (+0.22%) ▲|T24.51-0.15 (-0.61%) ▼|TMO583.43+7.02 (+1.22%) ▲|TMUS181.76-0.63 (-0.35%) ▼|TSLA303.21-4.23 (-1.38%) ▼|TXN271.38-5.69 (-2.05%) ▼|UBER69.78-0.96 (-1.36%) ▼|UNH425.23-3.56 (-0.83%) ▼|UNP292.38-2.07 (-0.70%) ▼|UPS104.47-1.06 (-1.00%) ▼|USB63.56-0.88 (-1.36%) ▼|V369.53+2.94 (+0.80%) ▲|VZ48.16-0.04 (-0.07%) ▼|WFC85.13-1.74 (-2.00%) ▼|WMT113.21+0.11 (+0.10%) ▲|XOM158.57+5.53 (+3.61%) ▲|AAPL341.32+1.24 (+0.36%) ▲|ABBV266.20+3.00 (+1.14%) ▲|ABT109.56+2.29 (+2.13%) ▲|ACN171.48+6.82 (+4.14%) ▲|ADBE258.88+9.70 (+3.89%) ▲|AMAT451.28-25.18 (-5.28%) ▼|AMD432.93-21.69 (-4.77%) ▼|AMGN395.09+1.99 (+0.51%) ▲|AMT175.97+4.47 (+2.61%) ▲|AMZN227.71-3.15 (-1.36%) ▼|AVGO375.10-5.82 (-1.53%) ▼|AXP333.82-2.81 (-0.83%) ▼|BA212.31-9.26 (-4.18%) ▼|BAC61.89-0.74 (-1.17%) ▼|BKNG200.00+0.69 (+0.35%) ▲|BLK1,101.76+4.21 (+0.38%) ▲|BMY63.65+0.05 (+0.08%) ▲|BNY154.89-1.60 (-1.02%) ▼|BRK-B510.00-2.37 (-0.46%) ▼|C128.77-3.70 (-2.79%) ▼|CAT803.28-37.57 (-4.47%) ▼|CL92.19-0.54 (-0.58%) ▼|CMCSA24.44+0.25 (+1.03%) ▲|COF211.67-0.74 (-0.35%) ▼|COP118.37+4.27 (+3.74%) ▲|COST973.24+6.66 (+0.69%) ▲|CRM183.83+2.33 (+1.28%) ▲|CSCO116.35+0.77 (+0.66%) ▲|CVS108.31-1.03 (-0.94%) ▼|CVX192.55+4.97 (+2.65%) ▲|DE620.23-19.62 (-3.07%) ▼|DHR201.84+2.79 (+1.40%) ▲|DIS98.92+0.03 (+0.03%) ▲|DUK130.08+0.84 (+0.65%) ▲|EMR148.48-3.33 (-2.19%) ▼|FDX310.13-2.51 (-0.80%) ▼|GD393.38+0.19 (+0.05%) ▲|GE356.32-7.28 (-2.00%) ▼|GEV923.17-20.21 (-2.14%) ▼|GILD133.38-0.94 (-0.70%) ▼|GM91.00+0.70 (+0.77%) ▲|GOOG331.19-1.41 (-0.42%) ▼|GOOGL332.34-1.37 (-0.41%) ▼|GS990.92-42.42 (-4.11%) ▼|HD338.33-6.14 (-1.78%) ▼|HON242.76-4.30 (-1.74%) ▼|IBM227.34-0.22 (-0.09%) ▼|INTC83.85-2.45 (-2.84%) ▼|INTU326.39+13.40 (+4.28%) ▲|ISRG356.63-5.17 (-1.43%) ▼|JNJ268.16+1.43 (+0.54%) ▲|JPM350.20-7.12 (-1.99%) ▼|KO90.72+2.45 (+2.78%) ▲|LIN509.84-1.34 (-0.26%) ▼|LLY1,223.45+2.79 (+0.23%) ▲|LMT578.65-2.66 (-0.46%) ▼|LOW216.07-2.18 (-1.00%) ▼|LRCX258.03-11.58 (-4.30%) ▼|MA564.48+1.73 (+0.31%) ▲|MCD271.71-1.31 (-0.48%) ▼|MDLZ65.59+3.11 (+4.98%) ▲|MDT87.80+0.92 (+1.06%) ▲|META586.87-6.54 (-1.10%) ▼|MMM181.61-0.88 (-0.48%) ▼|MO75.43+0.61 (+0.82%) ▲|MRK130.75-1.07 (-0.81%) ▼|MS205.87-5.71 (-2.70%) ▼|MSFT392.47-0.89 (-0.23%) ▼|MU788.34-32.19 (-3.92%) ▼|NEE89.79+0.51 (+0.57%) ▲|NFLX72.02-0.38 (-0.52%) ▼|NKE42.55-0.50 (-1.16%) ▼|NOW113.16+2.54 (+2.30%) ▲|NVDA191.44-5.57 (-2.83%) ▼|ORCL117.86-2.10 (-1.75%) ▼|PEP145.02+2.16 (+1.51%) ▲|PFE25.22-0.03 (-0.12%) ▼|PG145.28-3.61 (-2.42%) ▼|PLTR123.59+0.06 (+0.05%) ▲|PM201.15+0.98 (+0.49%) ▲|QCOM159.03-3.85 (-2.36%) ▼|RTX217.66-0.92 (-0.42%) ▼|SBUX103.59+0.49 (+0.48%) ▲|SCHW105.77-0.20 (-0.19%) ▼|SO97.13+0.35 (+0.36%) ▲|SPG237.22+0.52 (+0.22%) ▲|T24.51-0.15 (-0.61%) ▼|TMO583.43+7.02 (+1.22%) ▲|TMUS181.76-0.63 (-0.35%) ▼|TSLA303.21-4.23 (-1.38%) ▼|TXN271.38-5.69 (-2.05%) ▼|UBER69.78-0.96 (-1.36%) ▼|UNH425.23-3.56 (-0.83%) ▼|UNP292.38-2.07 (-0.70%) ▼|UPS104.47-1.06 (-1.00%) ▼|USB63.56-0.88 (-1.36%) ▼|V369.53+2.94 (+0.80%) ▲|VZ48.16-0.04 (-0.07%) ▼|WFC85.13-1.74 (-2.00%) ▼|WMT113.21+0.11 (+0.10%) ▲|XOM158.57+5.53 (+3.61%) ▲|
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Wednesday, July 29, 2026

Tag: infections

ENA Respiratory Receives USPTO Notice of Allowance for Two Patents Covering TLR2 Agonists and Rhinovirus-Mediated COPD Exacerbations

MELBOURNE, Australia, June 15, 2026 (GLOBE NEWSWIRE) -- ENA Respiratory, a clinical-stage pharmaceutical company developing innate immune modulators for the prevention of complications associated with respiratory viral infections in at-risk populations, announces today that it has received a Notice of Allowance from the U.S. Patent and Trademark Office (USPTO) for two patent applications, notably a composition-of-matter patent and method-of-use for its Toll-like receptor 2 (TLR2) therapies.

CARsgen Presents Allogeneic CAR T-cell Products CT0596 and CT1190B at EHA 2026

SHANGHAI, June 14, 2026 /PRNewswire/ -- CARsgen Therapeutics Holdings Limited (Stock Code: 2171.HK), a company focused on developing innovative CAR T-cell therapies, announces poster...

Menarini Group Reports Data from the Phase 3 SENTRY Trial of Selinexor (NEXPOVIO®) Plus Ruxolitinib in Myelofibrosis at The European Hematology Association (EHA) 2026...

FLORENCE, Italy and NEW YORK, June 14, 2026 (GLOBE NEWSWIRE) -- The Menarini Group (“Menarini”), a leading international pharmaceutical and diagnostics company, and Stemline Therapeutics, Inc. (“Stemline”), a wholly-owned subsidiary of the Menarini Group focused on bringing transformational oncology treatments to cancer patients, announced that new data related to the pivotal Phase 3 SENTRY trial will be presented as a late-breaking oral at The European Hematology Association (EHA) 2026 Congress.

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...

New TALVEY®▼(talquetamab) plus daratumumab data demonstrate the potential strength of a novel bispecific combination in earlier-line relapsed or refractory multiple myeloma

BEERSE, BELGIUM, June 13, 2026 (GLOBE NEWSWIRE) -- Johnson & Johnson today announced results from the investigational Phase 3 MonumenTAL-3 study.1 The results showed that TALVEY® (talquetamab), a GPRC5D bispecific antibody, in combination with daratumumab with or without pomalidomide demonstrated significant reduction in the risk of disease progression or death of up to 72.0%, and clinically meaningful reduction of up to 53.0% in the risk of death, compared to the standard regimen of daratumumab, pomalidomide, and dexamethasone (DPd) in patients with relapsed or refractory multiple myeloma (RRMM).1 Results showed a progression-free survival (PFS) rate of up to 81.3% versus standard of care (51.2%) and an overall survival (OS) rate of up to 89.2% versus standard of care (79.1%) at 24 months.1  

New TALVEY® (talquetamab-tgvs) plus DARZALEX FASPRO® (daratumumab and hyaluronidase-fihj) data demonstrate the strength of a bispecific combination in earlier-line relapsed or refractory multiple myeloma

TALVEY® plus DARZALEX FASPRO® with or without pomalidomide showed progression-free survival of up to 81% and overall survival of up to 89% at 24 monthsMonumenTAL-3 is the...

Traws Pharma Provides Regulatory Update on Influenza Program

NEWTOWN, Pa., June 12, 2026 (GLOBE NEWSWIRE) -- Traws Pharma, Inc. (NASDAQ: TRAW, the Company), a clinical-stage biopharmaceutical company developing novel therapies for critical global viral threats, today announced that the planned test of tivoxavir marboxil (TXM) in a Phase 2a human influenza challenge study has been deferred due to a negative review of the program by the United Kingdom’s Medicines and Healthcare Products Regulatory Agency (MHRA).

XORTX Announces Election to Voluntary Delist from the TSX Venture Exchange

CALGARY, Alberta, June 12, 2026 (GLOBE NEWSWIRE) -- XORTX Therapeutics Inc. ("XORTX" or the “Company”) (NASDAQ: XRTX | TSXV: XRTX | Frankfurt: ANU), a late-stage clinical pharmaceutical company focused on developing innovative therapies to treat gout and progressive kidney disease, announces that the Company has elected to voluntarily delist its common shares from the TSX Venture Exchange (“TSXV”). The Company will provide additional information on timing for the completion of the delisting of its common shares in a separate press release.

Akeso’s Gumokimab (AK111, Anti-IL-17) Approved by NMPA for Moderate-to-Severe Plaque Psoriasis, Bolstering Its Autoimmune Disease Portfolio

HONG KONG, June 11, 2026 /PRNewswire/ -- Akeso, Inc. (9926.HK) today announced that the National Medical Products Administration (NMPA) of China has approved gumokimab...

IMAAVY® (nipocalimab-aahu) demonstrates durable hemoglobin response and rapid onset of effect in pivotal Phase 2/3 study in warm autoimmune hemolytic anemia (wAIHA), an autoantibody-driven...

Patients in the IMAAVY 30 mg/kg treatment groupa achieved statistically significant durable hemoglobin responseb, with mean hemoglobin improvement of at least 1 g/dL as...

Fedora Pharmaceuticals Expands Scientific Advisory Board with Appointment of Drs. Michael Dudley, Keith Micetich, and Jürgen Bulitta

Drs. Michael N. Dudley, Keith A. Micetich, and Jürgen B. Bulitta join advisory board of renowned infectious disease leaders at Fedora Pharmaceuticals.

Ascendis to Showcase Advances in Treatment of Rare Endocrine Diseases at ENDO 2026

COPENHAGEN, Denmark, June 08, 2026 (GLOBE NEWSWIRE) -- Ascendis Pharma A/S (Nasdaq: ASND) today announced that the latest data from its Endocrinology Rare Disease programs in hypoparathyroidism, achondroplasia, and pediatric growth hormone deficiency will be shared in two oral presentations and three posters at ENDO 2026, the annual meeting of the Endocrine Society being held in Chicago from June 13-16, 2026.

PPMW launches summer Spill the Tea ambassadorship for Black Women

WASHINGTON, June 8, 2026 /PRNewswire/ -- In May, Planned Parenthood of Metropolitan Washington, DC launched the most recent cohort of its Spill the Tea...

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