Condition (MeSH)
Synostosis
ClinicalTrials.gov lists 92 trials for Synostosis or a narrower condition beneath it. Incyte Corporation has the most among industry and government lead sponsors, with 7.
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Trials per phase
3 of the 92 trials are tagged with Synostosis itself; the rest are tagged with a narrower condition beneath it.
When did Synostosis trials start? (25)
Shown in this order: most recent first, 1990 onwards. 2026 is partial: trials registered with a 2026 start date so far, not a full year.
Trials over time, by phase
- Phase 1
- Phase 1/2
- Phase 2
- Phase 3
- Phase 4
- Not applicable
- Observational
Top of scale: 12
Trials registered with a start date in each year, 1990 onward, stacked by phase (complete years only; the current partial year is in the table's notes). The table below lists the same counts, most recent years first.
| Year | Trials started |
|---|---|
| 2026 (partial year) | 5 |
| 2025 | 5 |
| 2024 | 7 |
| 2023 | 6 |
| 2022 | 5 |
| 2021 | 5 |
| 2020 | 12 |
| 2019 | 8 |
| 2018 | 2 |
| 2017 | 7 |
Showing 10 of 25 earlier years.
Forecast of the full-year count, planned starts included, not rows of this table: about 4 trials starting in 2026 and about 5 in 2027, the average of the 24 months through September, counted as registered and carried forward. The rows of this table count trials registered so far with a start date in the year, planned starts included; the forecast looks ahead to the count for the whole year, so it is not the same measure. In backtests on conditions of this size, forecasts made part-way through the year were typically off by about 28 percent and ran about 20 percent low against the count later registered; forecasts made before the year began were off by about 39 percent and ran about 37 percent low against the count later registered. These figures rest on a few years of history (target years from 2018 to 2025, varying by figure), place each condition as it is mapped today rather than as it was then, and score against a count for the newest year that was still being revised. Only condition series were scored. The 2026 forecast is below the 5 already registered with a 2026 start date: at the cutoff, 2 trials were already registered to start in October to December, more than the method's monthly average allows for, and the method does not use those planned starts.
Prediction, not a registry value: median of 36 months from start to primary completion across 6 trials still running at the 2026-10-09 snapshot; registered median of 34 months across 49 trials with a primary completion typed Actual. Source: ClinicalTrials.gov / AACT (CTTI), public domain.
What phase are Synostosis trials in? (7)
Shown in this order: phase order.
Show the trials by phase as a table
| Phase | Trials |
|---|---|
| Phase 1 | 9 |
| Phase 1/2 | 3 |
| Phase 2 | 15 |
| Phase 3 | 2 |
| Phase 4 | 3 |
| Not applicable | 24 |
| Observational | 36 |
How many Synostosis trials are recruiting? (9)
Shown in this order: the order a trial moves through, from not yet recruiting to unknown.
| Status | Trials |
|---|---|
| Not yet recruiting | 8 |
| Recruiting | 12 |
| Enrolling by invitation | 1 |
| Active, not recruiting | 6 |
| Completed | 40 |
Showing 5 of 9 statuses.
Status as registered on ClinicalTrials.gov. Each trial is counted once.
Which lead sponsors run the most Synostosis trials? (5)
Shown in this order: most trials first. Lead sponsors the registry classes as industry, NIH, US federal, other government or network. A hospital or university the registry files as government can appear here. Sponsors it classes as academic or other are shown on the full page, because that class cannot separate an institution from a named investigator.
| Sponsor | Trials |
|---|---|
| Incyte Corporation | 7 |
| National Human Genome Research Institute (NHGRI) | 6 |
| Janssen Research & Development, LLC | 3 |
| Basilea Pharmaceutica | 2 |
| Eisai Co., Ltd. | 2 |
Which drugs are being tested for Synostosis? (5)
Shown in this order: most trials first. One row per drug, matched to a single molecule under all its names, ranked by number of trials.
| Drug | Trials |
|---|---|
| Infigratinib | 3 |
| E7090 | 3 |
| Rogaratinib | 2 |
| PEMBROLIZUMAB | 2 |
| Aminocaproic Acid | 2 |
Interventions as named in the registry (10)
Shown in this order: most trials first.
| Drug | Trials |
|---|---|
| Pemigatinib Pill | 6 |
| acid tranexamic | 3 |
| Gemcitabine/Gemzar | 2 |
| Phase 1 Part B - dose expansion TYRA-200 taken once daily by mouth in 28-day cycles | 1 |
| Derazantinib 200 mg once daily + atezolizumab 1200 mg | 1 |
Showing 5 of 10 interventions.
These are the names sponsors entered on ClinicalTrials.gov that we have not matched to a single molecule. Some are drugs under a brand or code name; others are procedures, doses or arm labels.
Which serious adverse events do Synostosis trials report? (10)
Shown in this order: most subjects affected first. Subjects affected summed across trials, a cross-trial signal, not a rate.
| Adverse event | Subjects affected | Trials |
|---|---|---|
| Disease progression | 35 | 3 |
| Abdominal pain | 27 | 5 |
| Urinary tract infection | 27 | 4 |
| Acute kidney injury | 20 | 4 |
| General physical health deterioration | 20 | 3 |
Showing 5 of 10 adverse events.
Which publications cover Synostosis? (5)
Shown in this order: major-topic papers first, then newest, then most linked to trials.
| Publication | Journal | Year | Major topic |
|---|---|---|---|
| Radiographic assessment of congenital C2-3 synostosis. | Journal of orthopaedic surgery (Hong Kong) | 2010 | Yes |
| The manubriosternal joint--ananatomicoradiological survey. | Thorax | 1974 | Yes |
| Complications of intramedullary fixation of pediatric forearm fractures. | Journal of pediatric orthopedics | 1998 | No |
| The carrying angle in sex chromosome anomalies. | JAMA | 1974 | No |
| Variability of limb malformations induced by 5-fluoro-2'-deoxycytidine in mice. | Teratology | 1972 | No |
Sub-conditions in MeSH (4)
MeSH descendants one level down with at least one trial, most trials first.
Not on this page
Not measured: delivery record.
Checked, with nothing recorded for this condition: prevalence and rare-disease identity.