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Pharma & Biotech

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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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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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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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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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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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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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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Pharma & Biotech

Zai Lab’s August 6 earnings could reveal whether its 2026 commercial reset is starting to work

Zai Lab reports Q2 2026 results on August 6 as investors assess revenue pressure, COBENFY and TIVDAK launches, and zoci pipeline progress.

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Pharma & Biotech

SHASTA-3 and SHASTA-4 results support Arrowhead Pharmaceuticals’ planned plozasiran FDA filing

Arrowhead’s Phase 3 SHASTA data show deep triglyceride reductions and fewer pancreatitis events, supporting a planned 2026 U.S. filing.

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Pharma & Biotech

Can Tikva Allocell’s $8m bet solve the persistence problem holding back off-the-shelf CAR-T?

Tikva Allocell raises $8 million to advance TAVST01 toward an IND, testing an EBV-specific CAR-T approach for B7-H3-positive solid tumors.

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