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Representative image: A monitored sleep study and oral medication illustrate Incannex Healthcare’s DReAMzz Phase 2 screening program as the company refines IHL-42X dosing before a planned Phase 3 obstructive sleep apnea trial.
Pharma & Biotech

Incannex Healthcare begins DReAMzz screening to refine IHL-42X dosing before Phase 3 sleep apnea trial

Incannex Healthcare begins DReAMzz screening to select an IHL-42X dose before Phase 3. Read what the sleep apnea study must prove.

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Representative image: Clinical researchers review cardiopulmonary data and oral therapy options as Inhibikase Therapeutics advances IKT-001 in a pivotal Phase 3 trial for pulmonary arterial hypertension following FDA Orphan Drug Designation.
Pharma & Biotech

Inhibikase Therapeutics gains FDA orphan status for IKT-001 as pivotal PAH trial advances

Inhibikase Therapeutics wins FDA orphan status for IKT-001 as its pivotal PAH trial tests whether a prodrug can improve imatinib tolerability.

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Representative image: Laboratory researchers assess an oral blood disorder therapy as Nuvectis Pharma’s ciprocopan secures China approval for treatment-naive paroxysmal nocturnal hemoglobinuria.
Pharma & Biotech

Ciprocopan China approval gives PNH patients a new once-daily oral Factor B treatment option

Nuvectis Pharma’s ciprocopan wins China approval for PNH. Read how the once-daily Factor B drug could reshape the global treatment race.

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Amida’s Saraswati real-time HEDIS measurement platform is designed to help health plans track quality performance, identify care gaps and act before annual reporting deadlines. Representative image.
Medical Devices & Diagnostics

Can Amida’s Saraswati end the annual HEDIS scramble for health plans?

Amida’s Saraswati brings near-real-time HEDIS measurement to health plans, but adoption will depend on data quality, integration and trust.

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Biotechnology leaders and oncology researchers discuss next-generation cancer therapies as the Society for Immunotherapy of Cancer prepares its European immuno-oncology drug development summit in Lausanne. Representative image.
Pharma & Biotech

Europe’s immuno-oncology pipeline has a translation problem. Can SITC’s Lausanne summit fix it?

SITC’s Lausanne summit will connect regulators, biotech and academia to sharpen Europe’s path from immuno-oncology science to clinical trials.

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Eurofins Viracor’s BKV inSIGHT T-cell immunity panel is designed to support BK virus immune monitoring in kidney transplant patients by adding cellular immune-response insights to conventional viral-load testing. Representative image.
Medical Devices & Diagnostics

Can Eurofins Viracor’s BKV inSIGHT panel solve a dangerous kidney transplant monitoring blind spot?

Eurofins Viracor launches BKV inSIGHT for BK virus T-cell monitoring, but adoption will depend on validation and treatment-guidance evidence.

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CoSara begins clinical studies in India to evaluate Co-Diagnostics’ rapid PCR-based tuberculosis test, as the partners target faster near point-of-care TB detection. Representative image.
Medical Devices & Diagnostics

Can CoSara’s 30-minute PCR platform close India’s tuberculosis testing gap? The decisive studies have begun

CoSara begins India clinical studies of Co-Diagnostics’ rapid tuberculosis PCR test, but assay clearance and real-world validation remain ahead.

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Verastem Oncology advances its VS-7375 development programme as the TARGET-D 202 Phase 2 trial begins evaluating the investigational KRAS G12D inhibitor in previously treated advanced non-small cell lung cancer. Representative image.
Pharma & Biotech

Verastem has entered the KRAS G12D lung cancer race, but can VS-7375 close the evidence gap?

Verastem begins TARGET-D 202, testing 900 mg VS-7375 in previously treated KRAS G12D NSCLC, including a brain metastases cohort.

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Corcept Therapeutics’ second-quarter results will put early Lifyorli launch momentum, Korlym growth and the relacorilant FDA review under close scrutiny. Representative image.
Pharma & Biotech

Corcept Therapeutics sets July 29 Q2 call as Lifyorli launch and relacorilant review take centre stage

Corcept Therapeutics will report Q2 results on July 29, with Lifyorli launch sales, Korlym growth and relacorilant’s FDA review in focus.

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Affinia Therapeutics’ AFTX-201 gene therapy is advancing through the UPBEAT trial after receiving FDA Orphan Drug designation for BAG3-associated dilated cardiomyopathy. Representative image.
Pharma & Biotech

Affinia Therapeutics advances AFTX-201 gene therapy for BAG3 dilated cardiomyopathy

Affinia Therapeutics gains FDA orphan status for AFTX-201 as the UPBEAT trial tests gene therapy for BAG3 dilated cardiomyopathy.

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