Where clinical trials go wrong.

Almost every US trial is public. A 2007 law, FDAAA 801, makes registration mandatory, so the record is close to complete. A substantial protocol amendment costs about $450,000 in direct work (Tufts CSDD), before the weeks of delay each one adds. Multiply how often a company amends by how many trials it runs, and the pain sorts into an order. The companies at the top are losing the most. Here is the commercial case and its focus.

pain = mean( rank(amendments), rank(enrollment failure), rank(startup lag) )Each signal is ranked 0 to 100 against every other cell, then the three are averaged with equal weight. No learned weights, no black box. A cell with fewer than two measurable signals reads insufficient, not zero.
Less painMore paininsufficient data
Oncology8092927822,100
Infectious Disease205137459,765
Healthy Volunteers1819129,574
Endocrine & Metabolic84540446,264
Cardiovascular228172695,646
Neurology298086585,616
Immunology & Inflammation337868545,484
Psychiatry266451543,418
Respiratory116150593,366
General & cross-cutting127567542,899
Dermatology143127172,749
Rare & Genetic359588942,471
Nephrology & Urology87865342,222
Hematology289687922,155
Musculoskeletal365768611,854
Gastroenterology106745501,852
Ophthalmology367051421,624
Pain & Anesthesiology44139531,190
Women's & Reproductive Health74262841,007
In brief
What this is
An interactive map of 454,031 public trials, every figure carrying the sample it rests on (methodology).
The deliverables
The map with per-cell evidence, the ranked account list, and a one-page board brief (PDF).
How it is built
A deterministic pipeline over the public record. The amendment figure is a disclosed proxy, and contract research organizations are a named blind spot (limits).