1 / 3

Newly Launched First in Class LAG-3 Combination Drug Opdualag

Nivolumab Mechanism of Action: Antibody-dependent cell cytotoxicity; CD223 antigen inhibitors; Programmed cell death-1 receptor antagonists; T lymphocyte stimulants<br><br>Read for more information- https://www.delveinsight.com/asco-conference/article/lag-3-combination-drug-opdualag?utm_source=Promotion&utm_medium=ASCO&utm_campaign=ConferenceCoverage

yashb
Télécharger la présentation

Newly Launched First in Class LAG-3 Combination Drug Opdualag

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript


  1. [Document title] LAG-3 combination drug Opdualag: ASCO 2022 Bristol Myers Squibb presented a subgroup analysis from the RELATIVITY-047 trial for the newly approved OPDUALAG for the unresectable or metastatic melanoma patients. Nivolumab Mechanism of Action: Antibody-dependent cell cytotoxicity; CD223 antigen inhibitors; Programmed cell death-1 receptor antagonists; T lymphocyte stimulants Recently, FDA approved Opdualag, a fixed-dose combination of nivolumab and relatlimab for patients with previously untreated melanoma that cannot be removed surgically or has spread (metastasized) within the body. The Opdualag FDA approval was based on results from a large Phase II/III clinical trial (RELATIVITY-047). The clinical trial results have shown that Opdualag can double the time patients with previously untreated advanced melanoma can live without disease progression compared to Opdivo alone (the current SoC) without any added safety concerns. P a g e 1 | 3

  2. [Document title] Further Exploratory analyses by pre-specified subgroups from the RELATIVITY-047 trial were performed for PFS, OS, and ORR. As of the data cut-off date of October 2021 and media follow up of 19.3 months, OS, PFS and ORR continued to favour the combination of nivolumab + relatlimab over nivolumab across all key subgroups. The combination drug has shown superior pFS in key subgroups such as high tumor burden (HR: 0.7), metastatic M1c stage (HR: 0.83), LDH>ULN (2*ULN/ ≤ 2*ULN) (HR: 0.73-0.77), ECOG 0-1 (HR: ~0.80). Unstratified HR for OS in each of the aforementioned were as follows: 0.75; 0.78; 0- 76-0.93; 069-0.96 favoring nivolumab + relatilimab over nivolumab monotherapy. These results were consistent on ORR and supported nivolumab + relatlimab over nivolumab. KOL insights “Nivolumab plus relatlimab had a manageable safety profile, with no new or unexpected safety signals. These data further validate nivolumab plus relatlimab as a potential new treatment option in patients with advanced melanoma and support the benefit of dual checkpoint inhibition.”–Expert Opinion. Conclusion In March, Bristol Myers Squibb made history by introducing the first LAG-3 drug as part of an Opdivo combo called Opdualag as a treatment for patients with unresectable or metastatic melanoma. BMS’s plan to overcome the patent protection losses of Opdivo has succeeded as the clinical trial results have shown that Opdualag can double the time patients with previously untreated advanced melanoma can live without disease progression compared with Opdivo alone. Now BMS is planning to further delve into its landmark victory by presenting data on key subgroups (including those with poorer prognoses) to back its use in various melanoma patients. These results can further help BMS gain a positive perception from the KOL’s, establishing Opdualag as a new standard of care as first-line therapy in melanoma and enhancing its market size. First-line melanoma is just the first step BMS has planned for Opdualag. The Phase III RELATIVITY-098 trial assesses the Opdivo-plus-relatlimab cocktail versus Opdivo P a g e 2 | 3

  3. [Document title] alone in the post-surgery treatment of stages III–IV melanoma in the adjuvant setting. The company will soon launch a registrational study for the new combo in second- line colorectal cancer. The combination of nivolumab + relatlimab was favoured over nivolumab alone across key subgroups for PFS, OS, and ORR, and findings appeared consistent with outcomes in the overall population. Recommended- ASCO Conference 2020 | ASCO 2020 Abstracts | ASCO 2021 Highlights | ASCO Medical Conference | ASCO 2021 | ASCO 2021 Conference | when in ASCO 2021 | 2021 ASCO | ASCO US | ASCO 2022 Annual Meeting | ASCO Abstract 2022 | ASCO 2021 Abstract Read these Market Research Reports Viscosupplementation Devices Market | Transcatheter | Peripheral Nerve Repair Devices Market | Medical | Hypertrophic Cardiomyopathy Market | Allergic Dermatophagoides | Otitis Media Market | Transthyretin Amyloidosis Market | Intracranial Hemorrhage Market | GIST Pulmonary Infections Market | Inflammatory Pain Market | Intratumoral Cancer Therapies Market | Vascular Access Device Market | Pacemakers Market | Anti- Neutrophil Cytoplasmic Antibody-Associated | Avascular Necrosis Market | Pelvic Organ Prolapse Market Treatment Marijuana Asthma Market Market due to Farinae Market Market | Lice Infestations Market | Chronic Vasculitis Market P a g e 3 | 3

More Related