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Details:

KN035 is an investigational PD-L1 antibody, which is currently being evaluated for the treatment of undifferentiated pleomorphic sarcoma & myxofibrosarcoma.


Lead Product(s): Envafolimab,Ipilimumab

Therapeutic Area: Oncology Product Name: KN035

Highest Development Status: Phase IIProduct Type: Large molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable April 03, 2024

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IBI310 (anti-CTLA-4 monoclonal antibody) in combination with sintilimab (PD-1 inhibitor) is being evaluated for the treatment of MSI-H/dMMR Resectable Colon Cancer.


Lead Product(s): Ipilimumab,Sintilimab

Therapeutic Area: Oncology Product Name: IBI310

Highest Development Status: Phase IIIProduct Type: Large molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable March 26, 2024

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Combination of Opdivo (nivolumab) and Yervoy(Ipilimumab) met the main goal of a late-stage study evaluating it as an initial treatment for patients with advanced hepatocellular carcinoma.


Lead Product(s): Nivolumab,Ipilimumab

Therapeutic Area: Oncology Product Name: Opdivo

Highest Development Status: Phase IIIProduct Type: Large molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable March 20, 2024

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Ultimovacs UV1, which is a hTERT inhibitor, is being evaluated in Phase II clinical trial studies in combination with Ipilimumab and Nivolumab in patients for the treatment of Unresectable or Metastatic Malignant Melanoma.


Lead Product(s): UV1,Ipilimumab,Nivolumab

Therapeutic Area: Oncology Product Name: UV1

Highest Development Status: Phase IIProduct Type: Vaccine

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable March 07, 2024

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MaaT013 is a full-ecosystem, off-the-shelf, standardized, pooled-donor, enema Microbiome Ecosystem TherapyTM for acute, hospital use. It is being evaluated in combination with Ipilimumab for the treatment of metastatic melanoma.


Lead Product(s): MaaT013,Ipilimumab,Nivolumab

Therapeutic Area: Oncology Product Name: MaaT013

Highest Development Status: Phase IIProduct Type: Large molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable March 05, 2024

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UV1 is an off-the-shelf cancer vaccine designed to induce a specific T cell response against telomerase. It is being evaluated in phase 2 clinical trials in combination with ipilimumab and nivolumab for treatment of patients with unresectable malignant pleural mesothelioma.


Lead Product(s): UV1,Ipilimumab,Nivolumab

Therapeutic Area: Oncology Product Name: UV1

Highest Development Status: Phase IIProduct Type: Vaccine

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable February 19, 2024

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UV1 is an off-the-shelf cancer vaccine designed to induce a specific T cell response against telomerase. It is being evaluated in phase 2 clinical trials in combination with ipilimumab and nivolumab for treatment of patients with unresectable malignant pleural mesothelioma.


Lead Product(s): UV1,Ipilimumab,Nivolumab

Therapeutic Area: Oncology Product Name: UV1

Highest Development Status: Phase IIProduct Type: Vaccine

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable February 05, 2024

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UV1 is a universal cancer vaccine designed to induce a specific T-cell response against telomerase. It is under phase 2 clinical development in combination with nivolumab and ipilimumab for the treatment of unresectable or metastatic malignant melanoma.


Lead Product(s): UV1,Ipilimumab,Nivolumab

Therapeutic Area: Oncology Product Name: UV1

Highest Development Status: Phase IIProduct Type: Vaccine

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable January 16, 2024

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Opdivo (nivolumab) in combination with Yervoy (ipilimumab) is being evaluated in phase 3 clinical development for the treatment of microsatellite instability–high or mismatch repair deficient metastatic colorectal cancer.


Lead Product(s): Nivolumab,Ipilimumab

Therapeutic Area: Oncology Product Name: Opdivo

Highest Development Status: ApprovedProduct Type: Large molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable December 07, 2023

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Opdivo (Nivolumab) is a PD-1 Inhibitor antibody drug candidate, which is currently being evaluated in combination with "Ipilimumab" for the treatment of patients with microsatellite instability-high or mismatch repair deficient metastatic colorectal cancer.


Lead Product(s): Nivolumab,Ipilimumab

Therapeutic Area: Oncology Product Name: Opdivo

Highest Development Status: Phase IIIProduct Type: Large molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable December 07, 2023

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UV1 is a universal cancer vaccine designed to induce a specific T cell response against human telomerase, being developed in combination with the checkpoint inhibitors ipilimumab and nivolumab in the treatment of patients with unresectable or metastatic malignant melanoma.


Lead Product(s): UV1,Sargramostim,Ipilimumab

Therapeutic Area: Oncology Product Name: UV1

Highest Development Status: Phase IIProduct Type: Vaccine

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable November 02, 2023

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UV1 (telomerase inhibitor) in combination with ipilimumab and nivolumab is under phase 2 clinical development for first-line treatment of patients with metastatic malignant melanoma.


Lead Product(s): UV1,Sargramostim,Ipilimumab

Therapeutic Area: Oncology Product Name: UV1

Highest Development Status: Phase IIProduct Type: Vaccine

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable October 31, 2023

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Opdivo (nivolumab), a PD-1 blocking antibody, which is investigated in combination with Cisplatin-Based Chemotherapy Followed by Opdivo Demonstrates Significant Survival Benefits for Cisplatin-Eligible Patients with Unresectable or Metastatic Urothelial Carcinoma.


Lead Product(s): Nivolumab,Ipilimumab,Carboplatin

Therapeutic Area: Oncology Product Name: Opdivo

Highest Development Status: ApprovedProduct Type: Large molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable October 17, 2023

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UV1 is a universal cancer vaccine designed to induce a specific T cell response against human telomerase. UV1 has the potential to provide T cell support believed to be critical for triggering a strong anti-tumor immune response for the treatment of malignant melanoma.


Lead Product(s): UV1 Cancer Vaccine,Sargramostim,Ipilimumab

Therapeutic Area: Oncology Product Name: UV1

Highest Development Status: Phase IIProduct Type: Vaccine

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable October 12, 2023

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UV1 is a universal cancer vaccine designed to induce a specific T cell response against human telomerase. UV1 has the potential to provide T cell support believed to be critical for triggering a strong anti-tumor immune response for the treatment of mesothelioma.


Lead Product(s): UV1 Cancer Vaccine,Ipilimumab,Nivolumab

Therapeutic Area: Oncology Product Name: UV1

Highest Development Status: Phase IIProduct Type: Vaccine

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable October 09, 2023

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ImmunoBody® vaccines are designed to induce potent cytotoxic CD8 T cell responses against multiple epitopes via a dual mechanism of action. These DNA vaccines are being used both for the treatment of cancer.


Lead Product(s): SCIB1,Nivolumab,Ipilimumab

Therapeutic Area: Oncology Product Name: SCIB1

Highest Development Status: Phase IIProduct Type: Vaccine

Partner/Sponsor/Collaborator: Scancell

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable September 28, 2023

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KN035 (envafolimab) is a single-domain antibody against PD-L1 invented by Alphamab Oncology and licensed by TRACON, is the first approved subcutaneously injected PD-(L)1 inhibitor, which is investigated for MSI-H/dMMR advanced solid tumors.


Lead Product(s): Envafolimab,Ipilimumab

Therapeutic Area: Oncology Product Name: KN035

Highest Development Status: Phase IIProduct Type: Large molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable September 18, 2023

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Opdivo (nivolumab) in combination with cisplatin-based chemotherapy Shows statistically significant benefits in OS and PFS compared to standard-of-care cisplatin-based combinations as a first-line treatment for patients with unresectable or metastatic urothelial carcinoma.


Lead Product(s): Nivolumab,Ipilimumab

Therapeutic Area: Oncology Product Name: Opdivo

Highest Development Status: ApprovedProduct Type: Large molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable July 11, 2023

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KN035 (envafolimab) is a single-domain antibody against PD-L1 invented by Alphamab Oncology and licensed by TRACON, is the first approved subcutaneously injected PD-(L)1 inhibitor, which is investigated for MSI-H/dMMR advanced solid tumors.


Lead Product(s): Envafolimab,Ipilimumab

Therapeutic Area: Oncology Product Name: KN035

Highest Development Status: Phase IIProduct Type: Large molecule

Partner/Sponsor/Collaborator: Alphamab Oncology

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable June 20, 2023

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UV1 is a universal cancer vaccine designed to induce a specific T cell response against human telomerase. UV1 has the potential to provide T cell support believed to be critical for triggering a strong anti-tumor immune response for the treatment of Mesothelioma.


Lead Product(s): UV1 Cancer Vaccine,Sargramostim,Ipilimumab

Therapeutic Area: Oncology Product Name: UV1

Highest Development Status: Phase IIProduct Type: Vaccine

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable June 19, 2023

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The Phase 3 CheckMate -9LA trial demonstrating durable, long-term survival benefits with Opdivo (nivolumab) plus Yervoy (ipilimumab) with two cycles of chemotherapy compared to four cycles of chemotherapy alone in previously untreated patients with NSCLC.


Lead Product(s): Nivolumab,Ipilimumab,Carboplatin

Therapeutic Area: Oncology Product Name: Opdivo

Highest Development Status: ApprovedProduct Type: Large molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable June 04, 2023

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SQZ-AAC-HPV are derived from RBCs engineered with the Cell Squeeze® technology, designed to take advantage of the natural physiological process of aged RBC clearance by resident APCs in lymphoid organs which primes endogenous T cells to potentially drive antitumor activity.


Lead Product(s): SQZ-AAC-HPV,Ipilimumab,Nivolumab

Therapeutic Area: Oncology Product Name: SQZ-AAC-HPV

Highest Development Status: Phase IProduct Type: Cell and Gene therapy

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable March 22, 2023

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VAC85135, an investigational viral vector-based cancer vaccine for hematological malignancies. The MVA-based component of the vaccine was produced using ProBioGen's AGE1.CR.pIX.


Lead Product(s): VAC85135,Ipilimumab

Therapeutic Area: Oncology Product Name: VAC85135

Highest Development Status: Phase IProduct Type: Vaccine

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable January 20, 2023

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Envafolimab (KN035), a single-domain antibody against PD-L1 invented by Alphamab Oncology and licensed by TRACON, is the first approved subcutaneously injected PD-(L)1 inhibitor.


Lead Product(s): Envafolimab,Ipilimumab

Therapeutic Area: Oncology Product Name: KN035

Highest Development Status: Phase IIProduct Type: Large molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable December 14, 2022

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CPI-444 (ciforadenant) is an investigational small molecule, oral, checkpoint inhibitor designed to disable a tumor’s ability to subvert attack by the immune system by blocking the binding of adenosine in the tumor microenvironment to the A2A receptor.


Lead Product(s): Ciforadenant,Ipilimumab,Nivolumab

Therapeutic Area: Oncology Product Name: CPI-444

Highest Development Status: Phase I/ Phase IIProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable October 25, 2022

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The preclinical results showed that Comera’s caffeine-based SQore™ excipient did not result in local or systemic toxicity and had no impact on any measured pharmacokinetic (PK) parameters of ipilimumab when administered subcutaneously.


Lead Product(s): CLS-002,Ipilimumab

Therapeutic Area: Oncology Product Name: CLS-002

Highest Development Status: PreclinicalProduct Type: Large molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable October 18, 2022

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Envafolimab (KN035), a single-domain antibody against PD-L1 is the first approved subcutaneously injected PD-(L)1 inhibitor. Envafolimab is currently being studied in the ENVASARC Phase 2 and a Phase 3 pivotal trial in advanced biliary tract cancer patients.


Lead Product(s): Envafolimab,Ipilimumab

Therapeutic Area: Oncology Product Name: KN035

Highest Development Status: Phase IIProduct Type: Large molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable October 06, 2022

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Gavo-cel (TC-210) demonstrated a disease control rate (DCR) of 77%, which is defined in the Phase 1 portion of the trial as a response or sustained stable disease for at least three months post infusion.


Lead Product(s): Gavocabtagene Autoleucel,Nivolumab,Ipilimumab

Therapeutic Area: Oncology Product Name: TC-210

Highest Development Status: Phase I/ Phase IIProduct Type: Cell and Gene therapy

Partner/Sponsor/Collaborator: Bristol Myers Squibb

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable September 28, 2022

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By directing the immune system to hTERT antigens, UV1 drives CD4 helper T cells to the tumor to activate an immune system cascade and increase anti-tumor responses.


Lead Product(s): UV1,Ipilimumab

Therapeutic Area: Oncology Product Name: UV1

Highest Development Status: Phase IProduct Type: Vaccine

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable September 21, 2022

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The median progression-free survival (mPFS) among patients treated with UV1 and ipilimumab was 6.7 months, and the median overall survival (mOS) was 66.3 months.


Lead Product(s): UV1,Ipilimumab

Therapeutic Area: Oncology Product Name: UV1

Highest Development Status: Phase IProduct Type: Vaccine

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable September 12, 2022

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Cabometyx (cabozantinib) in combination with nivolumab and ipilimumab significantly reduced the risk of disease progression or death compared with the combination of nivolumab and ipilimumab.


Lead Product(s): Cabozantinib,Nivolumab,Ipilimumab

Therapeutic Area: Oncology Product Name: Cabometyx

Highest Development Status: Phase IIIProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable September 07, 2022

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Envafolimab (KN035), a single-domain antibody against PD-L1 invented by Alphamab Oncology, is the first approved subcutaneously injected PD-(L)1 inhibitor.


Lead Product(s): Envafolimab,Ipilimumab

Therapeutic Area: Oncology Product Name: KN035

Highest Development Status: Phase IIProduct Type: Large molecule

Partner/Sponsor/Collaborator: Runway Growth Capital LLC

Deal Size: Undisclosed Upfront Cash: Undisclosed

Deal Type: Financing September 06, 2022

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Comera announced favorable topline results of its SEQURUS-1 preclinical study in July, demonstrating supportive evidence of the safety of Comera’s lead caffeine-based proprietary SQore excipient when administered as a SQ biologic drug product formulation with a mAb.


Lead Product(s): Ipilimumab,Caffeine

Therapeutic Area: Oncology Product Name: Undisclosed

Highest Development Status: PreclinicalProduct Type: Large molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable August 11, 2022

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Envafolimab (KN035), a single-domain antibody against PD-L1 invented by Alphamab Oncology, is the first approved subcutaneously injected PD-(L)1 inhibitor.


Lead Product(s): Envafolimab,Ipilimumab

Therapeutic Area: Oncology Product Name: KN035

Highest Development Status: Phase IIProduct Type: Large molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable August 10, 2022

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Opdivo (nivolumab) and Yervoy (ipilimumab), combination was the first Immuno-Oncology combination to receive regulatory approval for the treatment of metastatic melanoma and is currently approved in more than 50 countries, including the United States and the European Union.


Lead Product(s): Nivolumab,Ipilimumab

Therapeutic Area: Oncology Product Name: Opdivo

Highest Development Status: Phase IIIProduct Type: Large molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable July 29, 2022

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SQore is a caffeine-based excipient when administered as a subcutaneous and combination ipilimumab, a mAb therapy that works to activate the immune system by targeting CTLA-4 to treat melanoma, as a model protein.


Lead Product(s): Caffeine,Ipilimumab

Therapeutic Area: Oncology Product Name: SQore

Highest Development Status: PreclinicalProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable July 13, 2022

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At a prespecified interim analysis for the secondary endpoint of overall survival (OS), the combination of Cabometyx (cabozantinib), nivolumab and ipilimumab versus the combination of nivolumab and ipilimumab did not demonstrate a significant benefit.


Lead Product(s): Cabozantinib,Nivolumab,Ipilimumab

Therapeutic Area: Oncology Product Name: Cabometyx

Highest Development Status: Phase IIIProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable July 11, 2022

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INITIUM has been designed as a robust comparative study to demonstrate that UV1 substantially enhances outcomes for patients over and above those that can be achieved with checkpoint inhibitors alone.


Lead Product(s): UV1,Nivolumab,Ipilimumab

Therapeutic Area: Oncology Product Name: UV1

Highest Development Status: Phase IIProduct Type: Vaccine

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable June 30, 2022

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Results from Phase 3 CheckMate -9LA trial demonstrating durable survival benefits with Opdivo (nivolumab) plus Yervoy (ipilimumab) with two cycles of chemotherapy compared to four cycles of chemotherapy in previously untreated patients with nSCLC.


Lead Product(s): Nivolumab,Ipilimumab

Therapeutic Area: Oncology Product Name: Opdivo

Highest Development Status: Phase IIIProduct Type: Large molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable June 06, 2022

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Opdivo (nivolumab) plus Yervoy-based combinations have shown significant improvements in OS in six Phase 3 clinical trials in five tumors to date: metastatic NSCLC, metastatic melanoma, advanced renal cell carcinoma, and esophageal squamous cell carcinoma.


Lead Product(s): Nivolumab,Ipilimumab

Therapeutic Area: Oncology Product Name: Opdivo

Highest Development Status: Phase IIIProduct Type: Large molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable June 06, 2022

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XmAb104 is engineered to selectively engage T cells that express both PD-1 and ICOS, important regulators of T cell activity, and we have observed biomarker activity consistent with engagement of both receptors.


Lead Product(s): XmAb23104,Ipilimumab

Therapeutic Area: Oncology Product Name: XmAb104

Highest Development Status: Phase IProduct Type: Large molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable May 26, 2022

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The data demonstrate that UV1 vaccination leads to dynamic immune responses in patients, notably the induction of memory T cells with a cytokine profile involving the production of IFN-gamma and TNF-alpha.


Lead Product(s): UV1,Ipilimumab

Therapeutic Area: Oncology Product Name: UV1

Highest Development Status: Phase IIProduct Type: Vaccine

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable May 25, 2022

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Tilsotolimod is an investigational, synthetic Toll-like receptor 9 agonist. Tilsotolimod (IMO-2125) has been shown to promote both innate (Type-I IFN, antigen presentation) and adaptive immune activation and may, in turn, contribute to tumor suppression and regression.


Lead Product(s): Tilsotolimod,Ipilimumab

Therapeutic Area: Oncology Product Name: IMO-2125

Highest Development Status: Phase IIIProduct Type: Large molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable May 17, 2022

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Opdivo (nivolumab) plus Yervoy-based combinations have shown improvements in OS in six Phase 3 clinical trials in five tumors to date, nSCLC, metastatic melanoma, advanced renal cell carcinoma, malignant pleural mesothelioma and esophageal squamous cell carcinoma.


Lead Product(s): Nivolumab,Ipilimumab

Therapeutic Area: Oncology Product Name: Opdivo

Highest Development Status: Phase IIIProduct Type: Large molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable May 16, 2022

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Measurable UV1-specific immune response in 91% of patients when combined with checkpoint inhibitor, as compared to 82% and 67% without checkpoint inhibitor.


Lead Product(s): UV1,Ipilimumab

Therapeutic Area: Oncology Product Name: UV1

Highest Development Status: Phase IIProduct Type: Vaccine

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable May 10, 2022

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SD-101, a potentially first-in-class, investigative TLR9 agonist, to reactivate the immune system within the liver and pancreas to enable more durable responses to other immunotherapeutics (e.g., checkpoint inhibitors) and improve patient outcomes.


Lead Product(s): SD-101,Ipilimumab,Nivolumab

Therapeutic Area: Oncology Product Name: SD-101

Highest Development Status: Phase I/ Phase IIProduct Type: Large molecule

Partner/Sponsor/Collaborator: The University of Texas MD Anderson Cancer Center

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable May 10, 2022

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SQZ-PBMC-HPV is being evaluated in a Phase 1/2 clinical trial for the treatment of HPV16+ advanced or metastatic solid tumors. Patients must be positive for the human leukocyte antigen serotype HLA-A*02.


Lead Product(s): SQZ-PBMC-HPV,Atezolizumab,Ipilimumab

Therapeutic Area: Oncology Product Name: SQZ-PBMC-HPV

Highest Development Status: Phase IProduct Type: Cell and Gene therapy

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable April 27, 2022

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Scope of patent, when issued, will cover cancer treatments that include UV1 peptide vaccine in combination with an anti-CTLA-4, anti-PD-1 or anti-PD-L1 antibody checkpoint inhibitor, it is expected that a patent will issue with a patent term up to at least June 2037.


Lead Product(s): UV1,Nivolumab,Ipilimumab

Therapeutic Area: Oncology Product Name: UV1

Highest Development Status: Phase IIProduct Type: Vaccine

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable April 22, 2022

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Result demonstrated highly tolerable safety profile and significantly higher objective response rate observed in lower weight patients in ENVASARC, to increase dose of envafolimab to 600 mg every three weeks, which is double the original envafolimab dose of 300 mg Q3W.


Lead Product(s): Envafolimab,Ipilimumab

Therapeutic Area: Oncology Product Name: KN035

Highest Development Status: Phase IIProduct Type: Large molecule

Partner/Sponsor/Collaborator: Alphamab Oncology

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable April 19, 2022

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The NMPA BTD for IBI310 was based on results from First part of a Phase 2 trial of IBI310 in combination with sintilimab showed potential for this combination as a new treatment option for patients in need.


Lead Product(s): Ipilimumab,Sintilimab

Therapeutic Area: Oncology Product Name: IBI310

Highest Development Status: Phase IIProduct Type: Large molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable April 14, 2022

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