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ClinicalTrials.gov 2 recruiting now early-phase tilt small index

Low Grade Ovarian Serous Adenocarcinoma: early-phase trial registry

2 of 3 indexed Low Grade Ovarian Serous Adenocarcinoma trials are currently recruiting, with more weight in Phase 1-2.

Corpus placement: #5,209 of 28,707 conditions by registered trial count.

3 US clinical trials · 2 currently recruiting · #5,209 of 28,707 conditions by registered trial count

Low Grade Ovarian Serous Adenocarcinoma: 3 US clinical trials tracked, 2 recruiting.

Low Grade Ovarian Serous Adenocarcinoma is the subject of 3 registered US clinical trials on ClinicalTrials.gov, 2 of them currently open to new participants. 0 are in Phase 3-4 (later-stage) and 2 in Phase 1-2 (earlier-stage). The most active sponsor is Verastem, running 1 of these trials.

Enrollment posture brief

Registry condition low-grade-ovarian-serous-adenocarcinoma

OPEN 2 | RECR 67% | LATE 0 | EARLY 2 | RANK #5209 | SPON 1

Nearest open-share peer: Acute Hypoxemic Respiratory Failure (67% recruiting · 6 trials)

Ablation80%ACL Reconstruction80%Low Grade Ovarian Serous (th…67%Abuse, Drug60%Acceptability60%
Open-enrollment share among volume-matched conditions near Low Grade Ovarian Serous Adenocarcinoma

Low Grade Ovarian Serous Adenocarcinoma lists 2 open slots (67% of 3 indexed trials). Peers are matched on registered volume, not therapeutic-area browse lists. How peer matching works →

Key findings

What ClinicalTrials.gov does not surface for Low Grade Ovarian Serous Adenocarcinoma on its own pages , computed from the registry mirror as of 2026-08-08. Each line carries its own denominator so it can be quoted as it stands.

  1. Low Grade Ovarian Serous Adenocarcinoma is recruiting above its size-band peers.

    2 of 3 indexed trials (66.7%) are open to enrollment, against a 46.5% average across 27,806 conditions with fewer than 20 trials. The peer set uses the same ClinicalTrials.gov-derived counts as this page.

Phase 22

Phase Distribution

PhaseTrial count
Phase 2 2

Top Sponsors

Named interventions

Most-linked intervention names on Low Grade Ovarian Serous Adenocarcinoma records (sponsor-reported on ClinicalTrials.gov). Counts are trial links, not unique products.

avutometinib (VS-6766) and defactinib Drug
1 trials
avutometinib (VS-6766) Drug
1 trials
Electronic Health Record Review Other
1 trials
Fulvestrant Drug
1 trials
nab-Sirolimus Drug
1 trials
Biospecimen Collection Procedure
1 trials

US sites by state

Facility locations filed on Low Grade Ovarian Serous Adenocarcinoma trials. A trial with sites in several states counts in each.

Texas 2 trials
Oklahoma 2 trials
Tennessee 1 trials
Oregon 1 trials
Ohio 1 trials
New York 1 trials
Nevada 1 trials
New Mexico 1 trials

Source: ClinicalTrials.gov, National Library of Medicine. Data is informational only.

What to do with this Low Grade Ovarian Serous Adenocarcinoma page

3 registered trials, 2 currently recruiting, is a starting point for a conversation, not a diagnosis or a recommendation.

  • 2 Low Grade Ovarian Serous Adenocarcinoma trials are currently recruiting, check eligibility criteria before contacting a site. Browse recruiting trials
  • Verastem sponsors the most Low Grade Ovarian Serous Adenocarcinoma trials on record, review their full trial history before evaluating a specific study. See Verastem's trials
  • Bring the specific trial ID (NCT number) to your own doctor before enrolling, this page is a directory, not medical guidance. Read the trial-finding guide

Trial and recruiting counts reflect ClinicalTrials.gov registry status as of the data vintage above; individual trial eligibility and enrollment status can change.

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This Low Grade Ovarian Serous Adenocarcinoma condition card totals 3 registered trials; most-linked intervention avutometinib (VS-6766) and defactinib; top US site state Texas. See our editorial standards & corrections policy, the methodology behind these numbers, the data changelog, or report a data error.