Renal Cancer Clinical Trial Pipeline Appears Robust With 75+ Key Pharma Companies Actively Working in the Therapeutics Segment | DelveInsight
24 sept. 2024 13h00 HE
|
DelveInsight Business Research LLP
New York, USA, Sept. 24, 2024 (GLOBE NEWSWIRE) -- Renal Cancer Clinical Trial Pipeline Appears Robust With 75+ Key Pharma Companies Actively Working in the Therapeutics Segment | DelveInsight ...
Le traitement prophylactique par dexaméthasone réduit les réactions liées à la perfusion chez les patients atteints d'un cancer du poumon non à petites cellules avancé muté EGFR et traités par RYBREVANT® ▼ (amivantamab) par voie intraveineu
13 sept. 2024 12h09 HE
|
Janssen Cilag International NV
La prémédication à une dose de 8 mg à entraîné un taux de réaction lié à la perfusion de 22,5 pour cent avec l'amivantamab par voie intraveineuse, soit trois fois moins que le taux de 67,4 pour cent...
RYBREVANT®▼ (amivantamab) en association avec le lazertinib montre une tendance très favorable en matière de survie globale par rapport à l'osimertinib dans le cancer du poumon non à petites cellules avancé muté par l’EGFR
11 sept. 2024 06h09 HE
|
Janssen Cilag International NV
De nouvelles données à plus long terme issues de l'étude MARIPOSA confirment les résultats supérieurs de l'association amivantamab plus lazertinib par rapport à l'osimertinib en monothérapie en tant...
Prophylactic dexamethasone regimen reduces infusion-related reactions in patients with EGFR-mutated advanced non-small cell lung cancer treated with intravenous RYBREVANT®▼ (amivantamab)
10 sept. 2024 18h20 HE
|
Janssen Cilag International NV
The 8 mg pre-medication regimen showed an infusion-related reaction rate of 22.5 percent with intravenous amivantamab, a three-fold reduction from 67.4 percent historically seen with standard IRR...
RYBREVANT®▼ (Amivantamab) plus Lazertinib zeigen einen starken positiven Trend beim Gesamtüberleben im Vergleich zu Osimertinib bei EGFR-mutiertem fortgeschrittenem Lungenkrebs
10 sept. 2024 13h04 HE
|
Janssen Cilag International NV
Neue Langzeitdaten aus der MARIPOSA-Studie bestätigen die überlegenen Ergebnisse der lazertinib-plus-lazertinib-Therapie im Vergleich zur Osimertinib-Monotherapie als Erstlinientherapie1 Ergebnisse...
Libtayo® (cemiplimab) Demonstrates Durable Survival Benefit at Five Years in Advanced Non-small Cell Lung Cancer
09 sept. 2024 17h00 HE
|
Regeneron Pharmaceuticals, Inc.
Late-breaking data at WCLC show Libtayo monotherapy nearly doubled median overall survival and reduced the risks of death and disease progression by 41% and 50%, respectively, compared to chemotherapy...
Boehringer’s zongertinib shows encouraging efficacy and tolerability profile in previously treated HER2 mutated lung cancer patients
09 sept. 2024 11h45 HE
|
Boehringer Ingelheim
Beamion LUNG-1, Phase Ib met its primary endpoint, demonstrating a meaningful objective response rate (ORR) of 66.7%, as assessed by blinded independent central review (BICR)1Preliminary activity in...
Regeneron to Highlight Progress Across Its Differentiated Oncology Portfolio and Pipeline at WCLC and ESMO
09 sept. 2024 07h00 HE
|
Regeneron Pharmaceuticals, Inc.
At WCLC, five-year survival data to be presented on Libtayo (PD-1 inhibitor) first-line monotherapy in advanced non-small cell lung cancer At ESMO, longer-term results with investigational fianlimab...
RYBREVANT®▼ (amivantamab) plus lazertinib show strong favourable overall survival trend versus osimertinib in EGFR-mutated advanced lung cancer
08 sept. 2024 14h30 HE
|
Janssen Cilag International NV
New longer-term data from the MARIPOSA study confirm superior outcomes of amivantamab plus lazertinib regimen compared to osimertinib monotherapy as first-line therapy1 ...
Boehringer Ingelheim to unveil groundbreaking oncology research at WCLC, demonstrating strength of portfolio
27 août 2024 03h05 HE
|
Boehringer Ingelheim
Data from the phase Ib Beamion LUNG-1 trial selected for late-breaking oral presentation in the Presidential Symposium at WCLC on Monday, September 9. The U.S. FDA and China's CDE have granted...