Phase IV

Pain & Anesthesiology

pain 53#36volume 135#73

Pain rank 36 of 76, volume rank 73 of 76 by industry trials. Trials here amend about 0.9x and fail enrollment about 1.9x the map median.

What this is worth

The amendment proxy, priced. Order of magnitude, anchor cited, assumptions on the table.

Per 100 industry trials in this cell, about 38 rewrite their eligibility criteria at least once. At the industry average of $450k direct cost per amendment, with the 6+ weeks of delay each not even counted, that is at least $17M at stake per 100 trials. Across the roughly 135 industry trials here, the floor is $23M.

If amendments fell by10%$2M30%$7M50%$11M

Assumes $450k direct cost per amendment (industry average; Phase II median runs lower, Phase III higher, and delay cost is excluded), applied to the proxy rate. The proxy counts only trials with at least one eligibility change, so this understates the true exposure. How this is derived.

The signals

Industry sponsors first, since that is the commercial buyer, each figure shown against the map median. All-sponsor figures follow. A trial counts as concluded once it has finished, whether completed, terminated or withdrawn.

Industry sponsors53pain index
Eligibility amendments
38%vs map 40%proxyn = 45sampled
Enrollment failure
26%vs map 13%n = 121concluded
Startup lag
36 dvs map 45.5 dn = 47with dates
Median duration
8.0 mon = 114completed
All sponsors34pain index
Eligibility amendments
29%proxyn = 86sampled
Enrollment failure
16%n = 1,710concluded
Startup lag
50 dn = 1,169with dates
Median duration
13.0 mon = 2,341completed
Why these trials stoppedlow accrual leads

The most common category here is low accrual (8 of 31 stopped). A keyword pass runs first; free text it could not place was sorted once by a frozen AI classification into these same categories, auditable rather than a live model. "No enrollment recorded (inferred)" is not a stated reason: it is read from a zero enrollment count, meaning the trial never enrolled anyone. "Not reported" means the sponsor left the field blank, shown rather than hidden.

Low accrual8 (26%)
Other stated reason6 (19%)
Sponsor decision5 (16%)
Not reported4 (13%)
External or regulatory3 (10%)
Safety or tolerability2 (6%)
No enrollment recorded (inferred)inferred1 (3%)
Feasibility or operational failure1 (3%)
Logistics or operations1 (3%)
n = 31terminated or withdrawn
Evidence12 trials

A sample of terminated or withdrawn trials in this cell. Each links to its ClinicalTrials.gov record.

TrialSponsorStatusStated reason
NCT05315479Baudax BioterminatedExternal or regulatory
NCT03927911Pacira Pharmaceuticals, IncterminatedFeasibility or operational failure
NCT03015961Pacira Pharmaceuticals, IncterminatedLow accrual
NCT02746263MallinckrodtterminatedLow accrual
NCT02680847PfizerterminatedSafety or tolerability
NCT02508935MallinckrodtterminatedSponsor decision
NCT02353754Pacira Pharmaceuticals, IncterminatedLow accrual
NCT02101554PfizerterminatedLow accrual
NCT01938547Chiesi Farmaceutici S.p.A.terminatedSponsor decision
NCT01919606Pacira Pharmaceuticals, IncterminatedLow accrual
NCT01919190Pacira Pharmaceuticals, IncterminatedSafety or tolerability
NCT01804673Janssen-Cilag G.m.b.HterminatedSponsor decision

Pain & Anesthesiology at other phases