AAPL323.85-3.89 (-1.19%) ▼|ABBV253.46-2.65 (-1.03%) ▼|ABT100.82+1.15 (+1.15%) ▲|ACN139.77-1.10 (-0.78%) ▼|ADBE220.19-6.98 (-3.07%) ▼|AMAT560.42-4.13 (-0.73%) ▼|AMD553.93+9.50 (+1.74%) ▲|AMGN367.44+1.20 (+0.33%) ▲|AMT166.14+2.75 (+1.68%) ▲|AMZN242.86-4.69 (-1.89%) ▼|AVGO396.13+9.63 (+2.49%) ▲|AXP348.86-1.94 (-0.55%) ▼|BA209.04+4.24 (+2.07%) ▲|BAC61.61+0.39 (+0.63%) ▲|BKNG179.21-0.19 (-0.11%) ▼|BLK1,044.79+6.55 (+0.63%) ▲|BMY60.84-0.10 (-0.16%) ▼|BNY159.81+0.92 (+0.58%) ▲|BRK-B489.28-0.37 (-0.08%) ▼|C132.83-0.01 (-0.01%) ▼|CAT898.25+8.28 (+0.93%) ▲|CL91.90+1.40 (+1.55%) ▲|CMCSA23.67-0.14 (-0.60%) ▼|COF201.62-4.60 (-2.23%) ▼|COP119.28+1.78 (+1.51%) ▲|COST924.51-4.72 (-0.51%) ▼|CRM162.70-7.36 (-4.33%) ▼|CSCO112.68+0.50 (+0.45%) ▲|CVS109.65-0.96 (-0.86%) ▼|CVX192.90+1.83 (+0.96%) ▲|DE608.21+21.33 (+3.63%) ▲|DHR177.48-1.53 (-0.85%) ▼|DIS96.47+0.33 (+0.34%) ▲|DUK127.86+1.95 (+1.55%) ▲|EMR139.90+0.64 (+0.46%) ▲|FDX319.12+3.93 (+1.25%) ▲|GD372.94+5.21 (+1.42%) ▲|GE341.95+1.25 (+0.37%) ▲|GEV993.30-85.51 (-7.93%) ▼|GILD131.50+1.22 (+0.94%) ▲|GM82.09+2.57 (+3.23%) ▲|GOOG345.87-0.32 (-0.09%) ▼|GOOGL346.53-0.62 (-0.18%) ▼|GS1,095.69+10.13 (+0.93%) ▲|HD332.81+1.21 (+0.36%) ▲|HON232.25+2.39 (+1.04%) ▲|IBM205.66-4.85 (-2.30%) ▼|INTC104.00-1.46 (-1.38%) ▼|INTU285.60-4.32 (-1.49%) ▼|ISRG343.74-6.33 (-1.81%) ▼|JNJ254.66+4.05 (+1.61%) ▲|JPM347.31+2.08 (+0.60%) ▲|KO82.55+0.58 (+0.70%) ▲|LIN510.57+5.54 (+1.10%) ▲|LLY1,163.58-11.84 (-1.01%) ▼|LMT516.18+9.09 (+1.79%) ▲|LOW204.00+1.74 (+0.86%) ▲|LRCX321.50-0.50 (-0.16%) ▼|MA533.26-5.04 (-0.94%) ▼|MCD264.20+0.29 (+0.11%) ▲|MDLZ60.82+0.96 (+1.60%) ▲|MDT81.82-0.54 (-0.65%) ▼|META626.35-17.46 (-2.71%) ▼|MMM170.45-0.32 (-0.18%) ▼|MO72.65-0.34 (-0.47%) ▼|MRK127.80+1.54 (+1.22%) ▲|MS218.35+1.95 (+0.90%) ▲|MSFT387.97-9.78 (-2.46%) ▼|MU971.29+0.47 (+0.05%) ▲|NEE89.60+1.67 (+1.90%) ▲|NFLX69.26+0.59 (+0.86%) ▲|NKE41.96-1.00 (-2.33%) ▼|NOW95.26-6.80 (-6.66%) ▼|NVDA213.69+6.40 (+3.09%) ▲|ORCL125.01-2.04 (-1.61%) ▼|PEP136.07+1.07 (+0.79%) ▲|PFE24.93-0.02 (-0.06%) ▼|PG149.76+1.66 (+1.12%) ▲|PLTR123.84-8.82 (-6.65%) ▼|PM192.80+4.76 (+2.53%) ▲|QCOM176.03+2.53 (+1.46%) ▲|RTX194.83+1.16 (+0.60%) ▲|SBUX104.17-0.28 (-0.27%) ▼|SCHW100.33+0.37 (+0.37%) ▲|SO95.54+1.69 (+1.80%) ▲|SPG226.82+0.03 (+0.01%) ▲|T23.03+0.77 (+3.44%) ▲|TMO524.26+0.80 (+0.15%) ▲|TMUS191.92+1.15 (+0.60%) ▲|TSLA375.83-3.11 (-0.82%) ▼|TXN294.06+2.76 (+0.95%) ▲|UBER70.45-1.10 (-1.54%) ▼|UNH434.68-1.67 (-0.38%) ▼|UNP293.46+0.33 (+0.11%) ▲|UPS116.44+0.10 (+0.09%) ▲|USB64.07+0.36 (+0.56%) ▲|V354.01-1.81 (-0.51%) ▼|VZ44.46+0.68 (+1.54%) ▲|WFC86.37-1.37 (-1.56%) ▼|WMT109.21-1.19 (-1.07%) ▼|XOM154.45+2.74 (+1.81%) ▲|AAPL323.85-3.89 (-1.19%) ▼|ABBV253.46-2.65 (-1.03%) ▼|ABT100.82+1.15 (+1.15%) ▲|ACN139.77-1.10 (-0.78%) ▼|ADBE220.19-6.98 (-3.07%) ▼|AMAT560.42-4.13 (-0.73%) ▼|AMD553.93+9.50 (+1.74%) ▲|AMGN367.44+1.20 (+0.33%) ▲|AMT166.14+2.75 (+1.68%) ▲|AMZN242.86-4.69 (-1.89%) ▼|AVGO396.13+9.63 (+2.49%) ▲|AXP348.86-1.94 (-0.55%) ▼|BA209.04+4.24 (+2.07%) ▲|BAC61.61+0.39 (+0.63%) ▲|BKNG179.21-0.19 (-0.11%) ▼|BLK1,044.79+6.55 (+0.63%) ▲|BMY60.84-0.10 (-0.16%) ▼|BNY159.81+0.92 (+0.58%) ▲|BRK-B489.28-0.37 (-0.08%) ▼|C132.83-0.01 (-0.01%) ▼|CAT898.25+8.28 (+0.93%) ▲|CL91.90+1.40 (+1.55%) ▲|CMCSA23.67-0.14 (-0.60%) ▼|COF201.62-4.60 (-2.23%) ▼|COP119.28+1.78 (+1.51%) ▲|COST924.51-4.72 (-0.51%) ▼|CRM162.70-7.36 (-4.33%) ▼|CSCO112.68+0.50 (+0.45%) ▲|CVS109.65-0.96 (-0.86%) ▼|CVX192.90+1.83 (+0.96%) ▲|DE608.21+21.33 (+3.63%) ▲|DHR177.48-1.53 (-0.85%) ▼|DIS96.47+0.33 (+0.34%) ▲|DUK127.86+1.95 (+1.55%) ▲|EMR139.90+0.64 (+0.46%) ▲|FDX319.12+3.93 (+1.25%) ▲|GD372.94+5.21 (+1.42%) ▲|GE341.95+1.25 (+0.37%) ▲|GEV993.30-85.51 (-7.93%) ▼|GILD131.50+1.22 (+0.94%) ▲|GM82.09+2.57 (+3.23%) ▲|GOOG345.87-0.32 (-0.09%) ▼|GOOGL346.53-0.62 (-0.18%) ▼|GS1,095.69+10.13 (+0.93%) ▲|HD332.81+1.21 (+0.36%) ▲|HON232.25+2.39 (+1.04%) ▲|IBM205.66-4.85 (-2.30%) ▼|INTC104.00-1.46 (-1.38%) ▼|INTU285.60-4.32 (-1.49%) ▼|ISRG343.74-6.33 (-1.81%) ▼|JNJ254.66+4.05 (+1.61%) ▲|JPM347.31+2.08 (+0.60%) ▲|KO82.55+0.58 (+0.70%) ▲|LIN510.57+5.54 (+1.10%) ▲|LLY1,163.58-11.84 (-1.01%) ▼|LMT516.18+9.09 (+1.79%) ▲|LOW204.00+1.74 (+0.86%) ▲|LRCX321.50-0.50 (-0.16%) ▼|MA533.26-5.04 (-0.94%) ▼|MCD264.20+0.29 (+0.11%) ▲|MDLZ60.82+0.96 (+1.60%) ▲|MDT81.82-0.54 (-0.65%) ▼|META626.35-17.46 (-2.71%) ▼|MMM170.45-0.32 (-0.18%) ▼|MO72.65-0.34 (-0.47%) ▼|MRK127.80+1.54 (+1.22%) ▲|MS218.35+1.95 (+0.90%) ▲|MSFT387.97-9.78 (-2.46%) ▼|MU971.29+0.47 (+0.05%) ▲|NEE89.60+1.67 (+1.90%) ▲|NFLX69.26+0.59 (+0.86%) ▲|NKE41.96-1.00 (-2.33%) ▼|NOW95.26-6.80 (-6.66%) ▼|NVDA213.69+6.40 (+3.09%) ▲|ORCL125.01-2.04 (-1.61%) ▼|PEP136.07+1.07 (+0.79%) ▲|PFE24.93-0.02 (-0.06%) ▼|PG149.76+1.66 (+1.12%) ▲|PLTR123.84-8.82 (-6.65%) ▼|PM192.80+4.76 (+2.53%) ▲|QCOM176.03+2.53 (+1.46%) ▲|RTX194.83+1.16 (+0.60%) ▲|SBUX104.17-0.28 (-0.27%) ▼|SCHW100.33+0.37 (+0.37%) ▲|SO95.54+1.69 (+1.80%) ▲|SPG226.82+0.03 (+0.01%) ▲|T23.03+0.77 (+3.44%) ▲|TMO524.26+0.80 (+0.15%) ▲|TMUS191.92+1.15 (+0.60%) ▲|TSLA375.83-3.11 (-0.82%) ▼|TXN294.06+2.76 (+0.95%) ▲|UBER70.45-1.10 (-1.54%) ▼|UNH434.68-1.67 (-0.38%) ▼|UNP293.46+0.33 (+0.11%) ▲|UPS116.44+0.10 (+0.09%) ▲|USB64.07+0.36 (+0.56%) ▲|V354.01-1.81 (-0.51%) ▼|VZ44.46+0.68 (+1.54%) ▲|WFC86.37-1.37 (-1.56%) ▼|WMT109.21-1.19 (-1.07%) ▼|XOM154.45+2.74 (+1.81%) ▲|
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Wednesday, July 22, 2026

Tag: treatment options

Desert Hope Treatment Center Launches First Responder Lifeline Program, Offering Confidential Care for Frontline Heroes

Desert Hope Treatment Center has launched its First Responder Lifeline Program for law enforcement officers, firefighters, and public safety professionals.

Teva Submits NDA for Ecopipam, a First-in-Class Investigational Therapy for Pediatric Tourette Syndrome

TEL AVIV, Israel, June 18, 2026 (GLOBE NEWSWIRE) -- Teva Pharmaceutical Industries Ltd. (NYSE and TASE: TEVA) today announced the submission of a New Drug Application (NDA) to the U.S. Food and Drug Administration (FDA) for ecopipam, a first-in-class investigational therapy for the treatment of pediatric Tourette syndrome.

Oncoinvent achieves 50% recruitment milestone in Phase 2 ovarian cancer study of Radspherin®

Strong recruitment momentum demonstrated in 2026 Year-to-date recruitment has already surpassed total enrollment for 2025OSLO, Norway, June 18, 2026 /PRNewswire/ -- Oncoinvent, a clinical-stage...

F2G and Shionogi Announce Positive Topline Results From Global Phase 3 OASIS Study Evaluating Oral Olorofim Versus AmBisome® Followed by Standard of Care in...


MANCHESTER, United Kingdom and OSAKA, Japan, June 18, 2026 (GLOBE NEWSWIRE) -- F2G Ltd and Shionogi & Co., Ltd (Head Office: Osaka, Japan; Chief Executive Officer: Isao Teshirogi, Ph.D) (“Shionogi”) today announced positive topline results from the global Phase 3 OASIS study (NCT05101187), comparing the investigational oral antifungal drug olorofim versus AmBisome® (liposomal amphotericin B for injection) followed by standard of care (SOC) in patients with invasive aspergillosis whose infection is either refractory to or unsuitable for azole therapy.

Alzheimer’s & Dementia Awareness Launches Nationwide

National Campaign Explores Advances in Early Detection, Research, Caregiving, and Brain HealthNEW YORK, June 17, 2026 /PRNewswire/ -- Mediaplanet today announces the launch of...

Azitra, Inc. to Present at 2026 BIO International Convention

BRANFORD, Conn., June 16, 2026 /PRNewswire/ -- Azitra, Inc. (NYSE American: AZTR), a clinical stage biopharmaceutical company focused on developing innovative therapies for precision...

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...

Ethyreal Bio Presents First Preclinical Data on ETHY-001 at ENDO 2026, Demonstrating Complete Blockade of Autoantibody Activation of TSHR and Differentiated Activity in TED

– ETHY-001 produced complete blockade of autoantibody-mediated TSHR activation across all patient serum samples tested, demonstrating breadth and consistency of effect –

Lundbeck presents new Phase II asedebart data in Cushing’s disease at ENDO 2026

Asedebart is an investigational monoclonal antibody designed to neutralize excess adrenocorticotropic hormone (ACTH) and reduce downstream cortisol production in Cushing's disease (CD)Urinary free cortisol...

Lundbeck presents new Phase II asedebart data in Cushing’s disease at ENDO 2026

Asedebart is an investigational monoclonal antibody designed to neutralize excess adrenocorticotropic hormone (ACTH) and reduce downstream cortisol production in Cushing's disease (CD)Urinary free cortisol...

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.

Mineralys Therapeutics Presents Late-Breaking Data on Lorundrostat and Heart Failure Risk Biomarkers at The Endocrine Society Annual Meeting (ENDO 2026)

– Lorundrostat was associated with significant reductions in heart failure risk biomarkers in a proteomic analysis of data from participants with uncontrolled hypertension –

Phase 3 Data Show TransCon® PTH Replicated Systemic Actions of Endogenous PTH Through Week 182 in Adults with Hypoparathyroidism

COPENHAGEN, Denmark, June 13, 2026 (GLOBE NEWSWIRE) -- Ascendis Pharma A/S (Nasdaq: ASND) today announced Week 182 data from its completed Phase 3 PaTHway Trial showing that long-term treatment with TransCon PTH (palopegteriparatide) demonstrated sustained efficacy and safety in adults with hypoparathyroidism. Over the three-and-a-half-year duration of the trial, TransCon PTH replicated the systemic actions of endogenous PTH, with a balanced, beneficial impact on the main target organ systems – CNS, kidney, small intestine, and bone – as demonstrated by improved quality of life and normalized and stable urine calcium, serum calcium, serum phosphate, and bone mineral density. These benefits were sustained while enabling independence from conventional therapy with active vitamin D and calcium.

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