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GST Reduction on Cancer Drugs: A Lifeline for Patients Battling Cancer

While the actual reduction in drug prices will depend on how manufacturers and distributors implement the GST cut, the potential savings could bring much-needed ...
Sep 17

Fewer Side Effects, Better Survival: IMRT Outperforms 3D-CRT in Lung Cancer Therapy

With better survival rates, fewer adverse effects, and enhanced precision, IMRT represents a significant step forward in lung cancer treatment....
Jul 02

Zumutor Biologics Advances Cancer Care with Novel Immunotherapy ZM008: A First-in-Class Anti LLT1 Antibody

As the ZM008-001 clinical trial progresses, the medical community eagerly awaits the results, which could lead the way for a new era in cancer ...
Jun 13

Silent Killer: How a Young Mother’s Vision Loss Led to a Lung Cancer Diagnosis

Despite having never smoked, she developed lung cancer that spread to her eyes, illustrating the unpredictable and invasive nature of the disease....
Jun 12

ImmixBio and BeiGene to evaluate combination of IMX-110 and Tislelizumab in solid tumors

Latest Pharma News Update...
Aug 31

Orpathys approved in China for patients with lung cancer and MET gene alterations

This approval follows a priority review designation by the Center for Drug Evaluation of China’s National Medical Products Administration (NMPA) and marks the first ...
Jun 23

Roche’s Tecentriq approved by European Commission for metastatic non-small cell lung cancer

Tecentriq is now the first and only single-agent cancer immunotherapy with three dosing options...
May 08

FDA Grants Fast Track Designation to Spectrum Pharmaceuticals’ Poziotinib

Poziotonib was also presented at European Society for Medical Oncology Targeted Anticancer Therapies (ESMO TAT) Virtual Congress 2021 ...
Mar 15

U.S. FDA expands approval of Pfizer’s LORBRENA as first-line treatment for ALK-Positive Metastatic Lung Cancer

In 2018, the FDA approved LORBRENA for the treatment of patients with ALK-positive metastatic NSCLC whose disease has progressed on crizotinib and at least ...
Mar 05

AtraZeneca's Imfinzi approved in the EU for less-frequent, fixed-dose use in unresectable non-small cell lung cancer

New option extends dosing from two to four weeks, reducing medical visits and improving patient convenience ...
Jan 15

PFIZER’S XALKORI APPROVED BY USFDA FOR ALK-POSITIVE ANAPLASTIC LARGE CELL LYMPHOMA IN CHILDREN AND YOUNG ADULTS

XALKORI is the first biomarker-driven therapy for relapsed or refractory ALCL in young people ...
Jan 15

Pfizer's LORBRENA sNDA in previously untreated ALK-positive lung cancer accepted for priority review by U.S. FDA

LORBRENA is a third-generation ALK inhibitor specifically developed to inhibit the most common tumour mutations that drive resistance to current medications and to address ...
Dec 29

Tagrisso approved in the US for the adjuvant treatment of patients with early-stage EGFR-mutated lung cancer

Approval based on unprecedented results from the ADAURA Phase III trial where Tagrisso reduced the risk of disease recurrence or death by 80%...
Dec 21

Amgen Submits Sotorasib New Drug Application To U.S. FDA For Advanced Or Metastatic Non-Small Cell Lung Cancer With KRAS G12C Mutation

Amgen today announced the submission of a New Drug Application (NDA) to the U.S. Food and Drug Administration (FDA) for sotorasib, an investigational KRASG12C ...
Dec 17

Imfinzi recommended for approval in the EU by CHMP for non-small cell lung cancer

This new dosing option is consistent with the approved Imfinzi dosing in extensive-stage small cell lung cancer and once approved, will be available to ...
Dec 15

Roche announces FDA approval of Gavreto for people with advanced or metastatic RET-mutant and RET fusion-positive thyroid cancers

Gavreto is a once-daily, oral precision therapy designed to selectively target RET alterations, including fusions and mutations...
Dec 03

RESULTS FROM PHASE 3 CROWN TRIAL OF PFIZER’S LORBRENA IN PREVIOUSLY UNTREATED ALK-POSITIVE LUNG CANCER PUBLISHED IN THE NEW ENGLAND JOURNAL OF MEDICINE

...
Nov 19

Bristol Myers Squibb Receives European Commission approval for Opdivo plus Yervoy for treatment of Lung Cancer

European Commission decision marks the first time a dual immunotherapy with limited chemotherapy is approved for patients with non-small cell lung cancer in the ...
Nov 09

Merck to acquire VelosBio

This acquisition is well positioned to achieve its maximum potential to benefit appropriate cancer patients in need...
Nov 06

FDA grants priority review of Regeneron-Sanofi's Libtayo for advanced Non-small Cell Lung Cancer

Libtayo is indicated for advanced non-smal cell cancer with PD-L1 Expression of ≥50%...
Oct 31

Roche receives US FDA approval for the cobas EGFR mutation test v2

Roche receives FDA approval for the cobas EGFR mutation test v2 as the first companion diagnostic test for expanded EGFR TKI therapies in patients with ...
Oct 30

Galera Therapeutics announces dosing of first patient for non-small cell lung cancer

Galera Therapeutics announces dosing of first patient in the phase 1/2 GRECO-1 clinical trial of GC4711 in combination with SBRT for non-small ...
Oct 23

WindMIL Therapeutics collaborates with Stephenson Cancer Center

WindMIL Therapeutics and Stephenson Cancer Center announce collaboration to collect bone marrow from patients with renal and urothelial carcinomas ...
Oct 14

Bristol Myers Squibbs get FDA approval for Opdivo and Yervoy : Malignant Pleural Mesothelioma

Opdivo + Yervoy is the first new systemic therapy in over 15 years to be approved by the FDA ...
Oct 03

FDA ACCEPTS SUPPLEMENTAL NEW DRUG APPLICATION FOR PFIZER’S XALKORI

Pfizer Inc. today announced that the U.S. FDA has accepted and granted priority review to the Company’s supplemental New Drug Application for XALKORI ...
Sep 23

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