Published: May 2022
Given the inherent expertise of CMOs and CDMOs, they are believed to be capable of enabling reduction in product development timelines, significant cost-benefits, as well as provide peptide developers access to larger production capacities and novel technologies
Roots Analysis has announced the addition of “Peptide Therapeutics Contract API Manufacturing Market (2nd Edition), 2022-2035” report to its list of offerings.
The incremental evolution in product discovery, clinical investigation and manufacturing methods have rendered outsourcing a crucial aspect of pharmaceutical development and production. Considering the various advantages associated with outsourcing certain operations, we are led to believe that the peptide therapeutics contract API manufacturing market is likely to witness positive growth in the coming years.
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More than 70 players offer contract manufacturing services to peptide therapeutic developers
Being an established segment of the peptide therapeutics industry, the contract manufacturing market is dominated (34%) by the presence of large companies (having more than 500 employees). Further, close to 83% of the CMOs offer method / analytical / process / assay development services for peptide therapeutics, across various scales of operations.
Over 100 peptide therapeutics contract API manufacturing facilities are established, worldwide
Close to 58% of the production facilities are located in the Asia Pacific region, followed by those based in Europe and North America. It is worth mentioning that majority of the facilities located in Asia Pacific have been established by large contract manufacturers.
415,000+ patients have been enrolled in over 1,300 clinical trials, worldwide
Clinical research activity, in terms of number of trials registered, is reported to have increased at a CAGR of 4.7%, in the past three years. Of the total number of trials, close to 66% of the studies have already been completed, while 20% are active and still recruiting patients.
More than 40 partnerships were reported in this industry, during 2014-2021
The partnerships and collaborations activity has grown at a CAGR of ~10.4% during the given period. Further, majority of the agreements were inked for the manufacturing of peptide therapeutics (42%), followed by those signed for product development (13%).
Expansion activity in this domain has grown at a CAGR of ~26%, between 2015 and 2021
Of the total, 71% instances were focused on expansion of dedicated capacities and facilities, followed by those carried out for enhancing existing capabilities, as well as establishment of new facilities (29%).
Global, installed peptide therapeutics contract API manufacturing capacity is currently estimated to be close to 291,700 liters
Majority share (close to 60%) of the global, installed capacity is captured by large players (more than 500 employees), at present. Moreover, close to 37% of the installed manufacturing capacity is available in the European region.
Strong clinical pipeline and upcoming patent expiries are anticipated to drive the demand for peptide therapeutics in the coming decade
The outsourced commercial demand for peptide therapeutics is projected to increase at a CAGR of 10.0%. Further, current clinical demand for peptide therapeutics captures around ~3.0% of the overall demand.
Increased access to advanced capabilities and technologies is anticipated to drive growth in this market at a CAGR of 13.6%, in the coming years
Based on type of peptide synthesis method used, majority of the revenue share (81%) is likely to be associated with the chemical approach. On the other hand, the peptide therapeutics contract API manufacturing market for non-chemical synthesis method(s) is expected to grow at a faster pace (CAGR of 15.4%), during the forecasted period.
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The financial opportunity within the peptide therapeutics contract API manufacturing market has been analyzed across the following segments:
The report also features inputs from eminent industry stakeholders, according to whom, manufacturing of small molecules is largely being outsourced due to exorbitant costs associated with setting-up of in-house expertise. The report includes detailed transcripts of discussions held with the following experts:
The research includes detailed profiles of key service providers (listed below) engaged in this domain; each profile features an overview of the developer, service portfolio, recent developments, and an informed future outlook.
For additional details, please visit
https://www.rootsanalysis.com/reports/view_document/peptide-therapeutics-manufacturing/305.html or email firstname.lastname@example.org
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