Enquirer Consulting Group
ProtaGene Buyer Map
Prepared for Gareth Sexton | ProtaGene | October 2026
As of Oct 7, 2026
ProtaGene runs analytical work for protein biologics and for cell and gene therapies, from research through to market. The companies developing those drugs are the buyers. This page sizes the US companies running open trials in each group, the US locations in the same industries, and the roles that usually sign off on outside analytical work. It says nothing about which of them ProtaGene already works with.
Companies leading an open cell or gene therapy trial with a US site
230
Industry lead sponsors, open studies.
Companies leading an open biologic drug trial with a US site, cell and gene aside
250
Antibodies, proteins, vaccines and other biologics.
Cell and gene companies whose open trials are all phase 1 or 2
170
No phase 3 open in the US.
Biotech research locations with 10 to 249 staff
1,800
US locations, 2023, contract labs included.
Trials running now
Industry-led studies in the federal trial registry, read on Oct 7, 2026.
| Group | Open studies | Companies leading them | Only phase 1 or 2 open | A phase 3 open |
|---|---|---|---|---|
| Cell and gene therapies | 410 | 230 | 170 | about 60 |
| Other biologics | 660 | 250 | 170 | about 70 |
US locations in the same industries
US biologic, drug and biotech research locations by staff size, mid-March 2023.
| Group | All locations | Under 10 staff | 10 to 49 staff | 50 to 249 staff | 250+ staff |
|---|---|---|---|---|---|
| Biologic product makers | 440 | 170 | about 100 | about 100 | about 80 |
| Drug makers | 1,400 | 570 | 380 | 320 | 180 |
| Biotechnology research and development firms | 5,700 | 3,700 | 1,200 | 530 | 140 |
What no public count reaches
Two groups this page cannot size, said in words rather than shown as a number.
Programs still in preclinical development, and contract manufacturers. A program shows up in the trial registry only once a study is filed, so programs still before their first trial sit outside the trial counts above, though their labs sit inside the location counts. Contract manufacturers that make biologics and viral vectors for developers are classed with the makers and research firms and cannot be separated from them. Each of these groups is built by name, company by company.
Who signs off
The roles that commonly own or weigh in on the choice of an outside analytical lab. Titles vary by company, and at the smaller ones one person often holds several.
| Group | Roles |
|---|---|
| Cell and gene therapy developers | Head of analytical development, VP of CMC, head of quality control, director of vector or process analytics, head of bioanalytical or translational sciences, head of external manufacturing |
| Biologic and biosimilar developers | Head of analytical development, director of characterization, VP of CMC, head of quality control, head of biosimilar development, R&D sourcing lead |
| Smaller biotechs | Chief scientific officer, VP of CMC (often one person covering analytics, process and quality), chief executive officer |
Three openings
Where the counts point.
Companies with a phase 3 open.
Smaller biotechs, where few people decide.
Denominators, definitions and sources
- Trial counts come from the federal trial registry, read on Oct 7, 2026. They count interventional studies with an intervention of the registry's genetic or biological type, that are open and name at least one US site, and whose lead sponsor is industry. Company names are matched after removing legal suffixes, so a company listed under two spellings, or a parent and its subsidiary, may count twice.
- Location counts are establishments in the federal annual count of business establishments by industry, 2023, national file, all legal forms. An establishment is one physical location with paid employees. Staff is paid employees at the location in the mid-March 2023 pay period. Where the file withholds a size cell, the withheld locations are recovered as the group total less the published cells.
- Industry codes 325414 biological product manufacturing, except diagnostic; 325412 pharmaceutical preparation manufacturing; 541714 research and development in biotechnology, except nanobiotechnology.
- Built from public registries, counts banded deliberately. Figures of 100 and over are rounded to two significant figures, figures from 10 to 99 to the nearest ten.
The named version of this page, the actual companies inside a row, is built one row at a time. If you want to walk through a row together, pick a time at cal.com/ecg. Prepared by Ben Beattie, ben@enquirerconsulting.com.
Enquirer Consulting Group | enquirerconsulting.com