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Representative image: An oncologist reviews lung scan images in a modern cancer care setting, reflecting Amgen’s EU approval for Imdylltra in relapsed extensive-stage small cell lung cancer.
Pharma & Biotech

Why Amgen’s Imdylltra EU approval could reshape second-line small cell lung cancer treatment

Find out how Amgen’s Imdylltra EU approval could change relapsed small cell lung cancer treatment across Europe.

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Representative image of an oncologist reviewing lung cancer scans in a modern treatment room, reflecting Amgen’s European approval for Imdylltra and the growing shift toward bispecific antibody therapies for extensive-stage small cell lung cancer.
Pharma & Biotech

Is Amgen’s bispecific lung cancer drug becoming a global standard after chemotherapy failure?

Amgen’s Imdylltra has European approval in relapsed small cell lung cancer. Survival data now face reimbursement and adoption tests.

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Representative image: A clinician reviews bladder cancer imaging in a modern oncology setting, reflecting Merck’s KEYTRUDA plus Padcev EU regulatory milestone for cisplatin-ineligible muscle-invasive bladder cancer patients.
Pharma & Biotech

Why Merck’s CHMP win for KEYTRUDA plus Padcev matters in muscle-invasive bladder cancer

Merck’s bladder cancer push is moving earlier in Europe. KEYTRUDA plus Padcev could reset cisplatin-ineligible MIBC care.

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Representative image: A haematology consultation illustrates how PYRUKYND’s European Union approval for adults with thalassaemia could shift attention toward oral rare blood disease treatments, patient access and reimbursement across Europe.
Pharma & Biotech

Could Agios and Avanzanite turn PYRUKYND into Europe’s next rare blood disease launch test?

PYRUKYND has EU approval in thalassaemia. Now Agios and Avanzanite face Europe’s harder test: access, uptake and reimbursement.

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Representative image: A healthcare professional prepares a subcutaneous injection in a clinical setting, reflecting the treatment shift highlighted by Pfizer’s Hympavzi EU indication expansion for hemophilia A and hemophilia B patients with inhibitors.
Pharma & Biotech

EU backs Pfizer’s Hympavzi for hemophilia patients with inhibitors. What changes now?

Hemophilia care is moving beyond factor replacement. Pfizer’s Hympavzi EU expansion tests how far anti-TFPI therapy can scale.

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Representative image: A clinical consultation for psoriatic arthritis, highlighting how Bristol Myers Squibb’s EU approval of Sotyktu could expand oral treatment options for adults with active inflammatory joint disease.
Pharma & Biotech

Why Bristol Myers Squibb’s Sotyktu approval could reshape the oral psoriatic arthritis race

A new EU approval is only the first hurdle. Sotyktu now faces Europe’s tougher test: payer access, sequencing, and real-world uptake.

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Pharma & Biotech

Does Rhythm Pharmaceuticals, Inc. now lead the rare neuroendocrine obesity treatment space?

Discover how Rhythm Pharmaceuticals, Inc.’s EU approval of setmelanotide could redefine rare obesity treatment and what comes next for the market.

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Pharma & Biotech

How Merck’s ENFLONSIA could challenge existing infant RSV prevention pathways in Europe

European Union approval gives Merck’s ENFLONSIA a new opening in infant RSV prevention. Read what it means for rollout, reimbursement, and competition.

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Meiji Seika Pharma advances morcamilast with EU orphan backing in rare dermatology
Pharma & Biotech

Meiji Seika Pharma wins EU orphan drug status for morcamilast in palmoplantar pustulosis

EU orphan status for morcamilast in PPP reshapes Meiji Seika Pharma’s European strategy. See what it means for PDE4 competition and rare dermatology.

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Pharma & Biotech

Novo Nordisk secures EU nod for higher Wegovy dose amid intensifying GLP-1 competition

EU approves 7.2 mg Wegovy for obesity. Explore what this means for efficacy, competition and reimbursement across Europe.

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