Likelihood of Approval and Phase Transition Success Rate Model – Camrelizumab in Metastatic Melanoma
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This report provides you with the data that allows you to track and predict the specific likelihood of approval (LOA) and phase transition success rate (PTSR) of a drug using GlobalData’s proprietary machine learning algorithms developed using over 10 years of historical data.
Camrelizumab in Metastatic Melanoma Drug Details:
Camrelizumab (Airuika) is a humanized monoclonal antibody acts as immunomodulatory agent. It is formulated as solution for intravenous route. Camrelizumab is indicated as third-line treatment for recurrent or refractory classical hodgkin’s lymphoma, advanced hepatocellular carcinoma patients with oxaliplatin system chemotherapy, combined with pemetrexed and carboplatin for epidermal growth factor receptor (EGFR) gene mutation negative and anaplastic lymphoma kinase (ALK) negative, non-resectable first-line treatment of locally advanced or metastatic non-squamous non-small cell lung cancer (NSCLC), locally advanced or metastatic esophageal squamous cell carcinoma patients who have previously received first-line chemotherapy and whose disease has progressed or become intolerable and for the treatment of patients with advanced nasopharyngeal carcinoma who had disease progression after previous second-line and above chemotherapy or intolerable treatment.Camrelizumab (SHR-1210) is under development for the treatment of advanced penile cancer, pancreatic ductal adenocarcinoma, gestational trophoblastic neoplasia, advanced or metastatic extrapulmonary neuroendocrine carcinomas, squamous cancer of nasal cavity and paranasal sinuses, advanced liver cancer, gastric cancer, esophageal cancer, gastroenteropancreatic neuroendocrine carcinoma, locally advanced head and neck squamous cell carcinoma, advanced androgen resistant prostate cancer, gestational trophoblastic neoplasia, advanced or metastatic esophageal squamous cell cancer, advanced chordoma, unresectable urothelial carcinoma of the renal pelvis, ureter, bladder, or urethra, advanced neuroendocrine tumors, glioblastoma multiforme, oral squamous cell carcinoma, advanced cervical neuroendocrine carcinoma (NEC), hypopharyngeal cancer, non-muscle invasive bladder cancer, relapsed or refractory diffuse large B cell lymphoma and follicular lymphoma, ALK-negative lung adenocarcinoma, relapsed or metastatic thyroid poorly differentiated or undifferentiated carcinoma, metastatic acral melanoma, advanced lung sarcomatoid carcinoma, metastatic biliary tract cancer, muscle-invasive bladder urothelial carcinoma, gastroesophageal junction adenocarcinoma, rectal cancer, metastatic triple-negative breast cancer, gastric cancer, recurrent or metastatic head and neck squamous cell carcinoma, gastroesophageal junction adenocarcinoma, esophageal cancer, squamous non-small cell lung cancer, hepatocellular carcinoma, esophageal squamous cell carcinoma, liver cancer, osteosarcoma, bile duct cancer, metastatic hepatocellular carcinoma, pancreatic cancer, soft tissue sarcoma, small-cell lung cancer, cervical cancer, renal cell carcinoma, transitional cell carcinoma, endometrial cancer, epithelial ovarian cancer, fallopian tube cancer, peritoneal cancer, metastatic colorectal cancer, melanoma, triple negative breast cancer, gynecological cancer, urinary tract cancer, anaplastic large cell lymphoma, advanced right-sided colon cancer, angioimmunoblastic T-Cell Lymphoma, peripheral T-Cell Lymphomas, metastatic periampulle cancer, bile duct cancer, gallbladder cancer, gastrointestinal tract cancer, relapsed or refractory extranodal NK/T cell lymphoma, papillary thyroid cancer, medullary thyroid cancer, synovial sarcoma, undifferentiated pleomorphic sarcoma, malignant fibrous histiocytoma, pleomorphic rhabdomyosarcoma, round cell liposarcoma, myxiod liposarcoma, malignant peripheral nerve sheath tumors, relapsed/refractory CD30+ lymphoma, naso-ocular related tumors, HER2 negative breast cancer, metastatic mucosal melanoma of head and neck (oral cavity, oropharynx, hypopharynx, or larynx) and solid tumor.It was also under development for the treatment of solid tumors including metastatic colorectal cancer, endometrial cancer, thymic carcinoma, malignant pleural mesothelioma, follicular thyroid cancer, human epidermal growth factor receptor 2 positive breast cancer (HER2+ breast cancer) and metastatic biliary tract cancer.
Report Coverage
The data is segmented by drug name per indication and shows the current likelihood of approval for the drug compared to the indication benchmark and the industry benchmark.
The Likelihood of Approval data is updated regularly based on events that take place which impact the clinical development process and regulatory considerations. GlobalData’s proprietary machine learning models consider these events in real time, to produce quantitative changes to the LOA and PTSR along with qualitative reasoning why the likelihood of approval has changed.
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Reasons to Buy
- Precise Likelihood of Approval and Phase Transition Success Rates: Our machine learning and proprietary models provide accurate predictions, helping you gauge the potential success of a drug in the regulatory process.
- Competitive Strategy Planning: Access information on LOA and PTSR for competitors’ drugs, allowing you to plan your clinical development, commercialisation and marketing strategies
- Event-driven Updates: Track event-driven changes in LOA and PTSR benchmarked against indication LOA/PTSR. Get the latest insights to adapt your strategies promptly!
- Well-informed Investment Decisions: This data helps you navigate the dynamic landscape of drug development and regulatory considerations.
Scope
- Drug Details: Drug name, Drug type, Intervention type
- Administration Pathway
- Therapeutic Areas
- Key Manufacturers
- Drug Development Status
This is an on-demand report that will be delivered upon request. The report will be delivered within 2 business days of the purchase, excluding weekends and holidays. Certain sections of the report may be removed or altered based on data availability and relevance.
Frequently asked questions
- Drugs which have been approved in the past 10 years
- Drugs which have failed during clinical development in the past 18 years
- Drugs which are currently in development
- Phase I, Phase II, Phase III, and Pre-Registration development stage
- Drugs must meet one of the following criteria to be included in the model:
- The developer has specified the US as an intended market for approval.
- The developer has not specified any country as an intended market for approval, i.e. the “Drug Geography” is listed as “Global”
- Innovator drugs and biosimilars
- Diagnostics, Imaging Agents, Biomarkers, stents and other drug delivery devices (covered in GlobalData’s Medical Intelligence Center).
- Nutraceuticals, dietary supplements, alternative medicines, imaging agents, radio emitter, transplants, transfusions, fillers, cosmetics, probiotics, antiseptics, antacids, mobilizing agents, veterinary drugs and drugs not seeking approval.
- Generic drugs
- Innovative drugs in Preclinical or Discovery Stage.
- Pipeline drugs sponsored by a Government or Institution.
- Drugs with a specific Drug Geography not the United States.
The probability of a drug ultimately receiving market authorization
The probability of a drug’s advancement to the next stage of clinical development
GlobalData’s Drug-Specific Likelihood of Approval (LoA) calculates the Phase Transition Success Rate (PTSR) and Likelihood of Approval (LoA) customized to individual drug. The model uses a combination of Machine Learning (ML) and a GlobalData proprietary algorithm to process data points from the Drugs, Clinical Trials, Regulatory Milestones, Company, and Financial databases.
Inclusion
Data Scope:
Drug Phase Scope:
Drug Geography Scope:
Drug Type Scope:
Entity Type Scope:
Only drugs in development by companies are included in the model.
Exclusion
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