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Jun 24

Is Paxalisib Better Than Temozolomide In The First-Line Setting?

Paxalisib better than Temozolomide? Paxalisib’s mechanism of action involves directly suppressing PI3K in the PI3K/AKT kinase (also known as protein kinase B) signalling pathway, which prevents the PI3K signalling pathway from being activated. In sensitive tumour cell populations, this may prevent both cell growth and survival. When used as first-line…

2 min read

Is Paxalisib Better Than Temozolomide In The First-Line Setting?
Is Paxalisib Better Than Temozolomide In The First-Line Setting?

Jun 24

Elranatamab exhibits a 60.6% ORR and a tolerable safety profile, according to new results from a planned interim analysis of the Phase II MagnetisMM-3 registration-enabling study

Pfizer Presents First Data from Planned Interim Analysis of Pivotal Phase II MagnetisMM-3 Trial of BCMA-CD3 Bispecific Antibody Elranatamab (PF-06863135) Mechanism of Action: Binds BCMA on myeloma cells and CD3 T cells, thereby bringing together T cells and activating them in the vicinity of the myeloma cell resulting in cell…

4 min read

Elranatamab exhibits a 60.6%
Elranatamab exhibits a 60.6%

Jun 23

Sanofi’s ADC is targeting CEACAM5 in patients with NSCLC

Phase I/II study of tusamitamab ravtansine (Sanofi) in patients with non-sq having locally advanced or metastatic NSCLC for which no standard alternative therapy is available. Tusamitamab ravtansine (SAR408701) is an ADC composed of a humanized monoclonal antibody that binds carcinoembryonic antigen-related cell adhesion molecule-5 (CEACAM5) and a cytotoxic maytansinoid that…

2 min read

Sanofi’s ADC is targeting CEACAM5 in patients with NSCLC
Sanofi’s ADC is targeting CEACAM5 in patients with NSCLC

Jun 23

Performance of Veru Pharma’s Sabizabulin in Phase I/II mCRPC Trial

In the Phase Ib/II clinical trial of Sabizabulin in men with metastatic castration-resistant prostate cancer, Veru published important findings. Sabizabulin Mechanism of Action: Tubulin inhibitors; Tubulin polymerization inhibitors The alpha and beta-tubulin subunits of cellular intermediate filaments and microtubules are targeted, bound, and crosslinked by the first-in-class small chemical sabizabulin…

3 min read

Performance of Veru Pharma’s Sabizabulin in Phase I/II mCRPC Trial
Performance of Veru Pharma’s Sabizabulin in Phase I/II mCRPC Trial

Jun 21

Is GSK’s Jemperli giving us reason to believe that cancer can be beaten? It’s incredible to have a response rate of 100%

Every Patient in a Drug Trial Has Their Rectal Cancer Disappear In mismatch repair-deficient locally advanced rectal cancer, single-agent PD-1 blocking as a curative-intent treatment A total of 30 patients with clinical stage II and III dMMR rectal cancer will be enrolled in the single-arm Phase II study of dostarlimab…

2 min read

Is GSK’s Jemperli giving us reason to believe that cancer can be beaten?
Is GSK’s Jemperli giving us reason to believe that cancer can be beaten?

Jun 16

CEL-SCI Corporation Presents First-of-its-Kind Results For Lower-Risk Advanced Primary SCCHN Population in 25+ Years Through Its Phase III IT-MATTERS Study

ASCO 2022 Conference: Phase III IT-MATTERS study Highlights CEL-SCI’s leukocyte interleukin injection is an immunity booster for patients with Head and Neck squamous cell carcinoma! Multikine is CEL-SCI’s lead investigational immunotherapy product being developed as a potential first-line neoadjuvant therapy in patients with advanced primary squamous cell carcinoma of the…

3 min read

CEL-SCI Corporation Presents First-of-its-Kind Results For Lower-Risk Advanced Primary SCCHN…
CEL-SCI Corporation Presents First-of-its-Kind Results For Lower-Risk Advanced Primary SCCHN…

Jun 14

Trodelvy met the primary endpoint in the TROPiCS02 study in extensively pretreated HR+/HER2 breast cancer patients

In a Phase III trial, Gilead Sciences’ Trodelvy met the primary endpoints, lowering the probability of disease progression or death by 30%. In TROPiCS-02, Trodelvy was compared to chemotherapy in third-line HER2+, ER+ breast cancer. …

4 min read

Trodelvy met the primary endpoint in the TROPiCS02 study in extensively pretreated HR+/HER2 breast…
Trodelvy met the primary endpoint in the TROPiCS02 study in extensively pretreated HR+/HER2 breast…

Jun 10

Pluvicto, Novartis’ first licenced radioligand therapy for PSMA-positive mCRPC, will be the subject of a subgroup analysis

Pluvicto (177Lu-PSMA-617) was the first FDA-approved targeted radioligand therapy (RLT) for eligible patients with mCRPC in March 2022. Pluvicto (177Lu-PSMA-617) is a combination of a targeting chemical (ligand) and a therapeutic radioisotope. The FDA granted approval based on the results of the pivotal Phase III VISION trial, which showed a…

4 min read

Pluvicto, Novartis’ first licenced radioligand therapy for PSMA-positive mCRPC, will be the subject…
Pluvicto, Novartis’ first licenced radioligand therapy for PSMA-positive mCRPC, will be the subject…

Jun 9

Genmab/Abbvie’s Epcoritamab Achieves a 100% Response Rate In Patients With R/R Follicular Lymphoma

The efficacy and safety data for epcoritamab will be presented by Genmab and Abbvie. What is the market position of the antibody in Florida? EPCORE NHL-2 is a Phase Ib/II study in R/R FL that looks at the safety and preliminary efficacy of epcoritamab in combination with other drugs. Epcoritamab…

3 min read


Jun 9

A Quick Overview of Diffuse Large B-Cell Lymphoma (DLBCL) at ASCO 2022

Diffuse Large B Cell Lymphoma is a deadly blood cancer that is the most frequent kind of non-Hodgkin lymphoma (NHL), with over 40,000 new cases diagnosed in Europe each year and another 25,000 in the United States. While the ASCO 2022 annual meeting is approaching, pharma behemoths such as Seagen…

3 min read

Haven Smith

Haven Smith

I am writer. I write about pharma diseases

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