The Receptor Activity Modifying Protein 1 pipeline drugs market research report outlays comprehensive information on the Receptor Activity Modifying Protein 1 targeted therapeutics, complete with analysis by indications, stage of development, mechanism of action (MoA), route of administration (RoA), and molecule type. GlobalData’s report assesses the drugs in the Receptor Activity Modifying Protein 1 pipeline by therapy areas, indications, stages, MoA, RoA, molecule type and the key players in the development pipeline. Buy the report here.

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The report also covers products from therapy areas such as Metabolic Disorders, and Gastrointestinal which include the indications Type 2 Diabetes, Obesity, and Metabolic Dysfunction-Associated Steatohepatitis (MASH). It also reviews key players involved in Receptor Activity Modifying Protein 1 targeted therapeutics development with respective active and dormant or discontinued products.

The Receptor Activity Modifying Protein 1 pipeline targets constitutes close to seven molecules. Out of which, approximately seven molecules are developed by companies and the remaining by the universities/institutes. The molecules developed by companies in Phase III, Phase II, Preclinical, and Discovery stages are 2, 2, 2, and 1 respectively.

Receptor Activity Modifying Protein 1 overview

Receptor activity modifying protein 1 (RAMP1) is a member of the RAMP family of single-transmembrane-domain proteins, called receptor (calcitonin) activity modifying proteins (RAMPs). RAMP1 acts as a receptor for calcitonin-gene-related peptide (CGRP) together with CALCRL and transports the calcitonin gene-related peptide type 1 receptor (CALCRL) to the plasma membrane.

For a complete picture of Receptor Activity Modifying Protein 1’s drug pipeline, buy the report here.

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Global Markets Direct’s report features investigational drugs from across globe covering over 20 therapy areas and nearly 3,000 indications. The report is built using data and information sourced from Global Markets Direct’s proprietary databases, company/university websites, clinical trial registries, conferences, SEC filings, investor presentations and featured press releases from company/university sites and industry-specific third-party sources.

Drug profiles featured in the report undergo periodic review following a stringent set of processes to ensure that all the profiles are updated with the latest set of information. Additionally, various dynamic tracking processes ensure that the most recent developments are captured on a real time basis.