Skip to content
Pharma Observatory a Scientist.com platform

Organization (Industry)

VERU INC.

ClinicalTrials.gov lists VERU INC. as lead sponsor of 12 trials. It has 20 active development programs and 3 approved assets.

US Industry Manufacturer CIK 0000863894
Email me this page as a PDF

Search trials, drugs, companies and investigators, and follow each one to the others. Individual plan, $249/seat/mo. Card required.

5 0 2018 2026

Trials started per year with this organization as sponsor or collaborator, 1990 onward. The series also counts trials where the organization is a collaborator; the lead-sponsor trial count does not.

2026 is partial: 1 registered with a 2026 start date. The dashed outline is the pace from the 1 registered with a start date through September, planned starts included, not adjusted; not a forecast. No forecast is made for this organization: it averages 1.2 trial starts a year over the five years to September, under the 5 a year the method needs.

This page covers VERU INC.: 12 lead-sponsored trials and 2 legal-entity registrations.

Get the VERU INC. report as a PDF

The PDF carries up to 50 rows of each section, where the page shows the first few, with the sources listed. Enter a work email and confirm it from the message we send, and the report follows by email.

Disease areas (10)

Shown in this order: most trials first.

Disease areas
Disease area Trials
Breast Neoplasms 4
Obesity 2
Bulbo-Spinal Atrophy, X-Linked 1
Muscular Atrophy 1
Muscular Atrophy, Spinal 1

Trials by start year as sponsor or collaborator (8)

Shown in this order: most recent first. 2026 is partial: trials registered with a 2026 start date so far, not a full year.

Show the table of trials by start year as sponsor or collaborator
Trials by start year as sponsor or collaborator
Year Trials started
2026 (partial year) 1
2024 1
2023 1
2022 1
2021 5
2020 1
2019 1
2018 1

Recruitment duration, a model prediction: 1 trial still running at the 2026-10-09 snapshot, fewer than the 5 needed for a median. Source: ClinicalTrials.gov / AACT (CTTI), public domain.

Active development programs (20)

Shown in this order: max phase, then active trials.

Active development programs
Drug Disease area Max phase Trials
VERU-111 Severe Acute Respiratory Syndrome Phase 3 1
non-steroidal AI, or steroidal AI (exemestane with or without everolimus) or Fulvestrant Breast Neoplasms Phase 3 1
Enobosarm & Abemaciclib Combo Breast Neoplasms Phase 3 1
VERU-111 Prostatic Neoplasms Phase 3 1
VERU-111 Prostatic Neoplasms, Castration-Resistant Phase 3 1

Approved assets (3)

Shown in this order: max phase first.

Approved assets
Drug Trials
Exemestane 1
Semaglutide 1
Sacituzumab Govitecan 1

Sponsor delivery record (1)

Enrollment hit target: the share of this sponsor's lead-sponsored trials whose actual enrollment reached the planned enrollment. On time: the share whose actual primary completion date was no later than the planned date. Each share counts only trials where we observed an estimated figure before the actual one, and n is that number of trials. Below 5 trials the count is shown as a fraction, not a percentage.

Sponsor delivery record
Enrollment Timeline
27% hit target (n=11) 11% on time (n=9)

Journals published in (1)

Journals published in
Journal Publications
NEJM evidence 1

US granted patents (1)

Patents are not classified by disease area in the source, so this is the organization's overall portfolio, not a split by disease.

US granted patents
US patents granted Granted in the last 5 years Most recent grant
2 2 2025-03-04

SEC-reported annual financials (11)

Shown in this order: newest fiscal year first; SEC EDGAR XBRL companyfacts, USD as reported.

SEC-reported annual financials
Fiscal year Revenue (USD) Net income (USD) R&D (USD)
2025 not reported -22,726,279 15,588,185
2024 16,886,419 -37,801,426 12,782,167
2023 16,296,958 -93,152,692 51,202,219
2022 39,354,352 -83,776,020 70,646,103
2021 61,259,528 7,394,374 32,694,405
2020 42,592,060 -18,973,535 16,935,222
2019 31,803,387 -12,017,366 13,743,826
2018 15,864,483 -23,938,389 10,850,958
2017 13,655,592 -6,612,047 3,076,390
2016 22,127,342 344,725 99,393

Financing and grant events (32)

Shown in this order: most recent first.

Financing and grant events
Date Round type Amount (USD) Source
2026-07-02 ATM offering not disclosed Sec extracted
2026-04-07 Follow-on offering 50,407,000 Edgar offerings
2026-04-07 Follow-on offering 200,000,000 Edgar offerings
2025-10-30 Other financing not disclosed Edgar offerings
2025-10-30 Public offering not disclosed Sec extracted

FDA inspection record (1)

FDA inspection record
Latest classification Inspections
VAI 1

Climate targets, as filed (1)

Climate targets, as filed
Reporting year Net-zero target
FY2022 not disclosed

Workforce and board diversity, as filed (1)

Workforce and board diversity, as filed
Reporting year Workforce % women Board % women
2025 not disclosed not disclosed

Latest dated events (48)

Shown in this order: newest first.

Latest dated events
Date Event Source
2026-07-02 At-the-market offering Funding rounds and grants (NIH RePORTER + SEC EDGAR)
2026-04-07 Follow-on offering Funding rounds and grants (NIH RePORTER + SEC EDGAR)
2026-04-07 Follow-on offering Funding rounds and grants (NIH RePORTER + SEC EDGAR)
2026-03-26 Trial started Clinical trials (ClinicalTrials.gov) (ClinicalTrials.gov, U.S. National Library of Medicine; AACT database, Clinical Trials Transformation Initiative (CTTI))
2025-10-30 Financing Funding rounds and grants (NIH RePORTER + SEC EDGAR)

Biomarker capability evidence (69)

Shown in this order: tier desc, then gene symbol.

Biomarker capability evidence
Gene Role Evidence
AR Trial sponsor Named in trial inclusion criteria
AR Trial sponsor Named in trial inclusion criteria
AR Trial sponsor Named in trial inclusion criteria
AR Trial sponsor Primary endpoint in a Phase 3 trial
AR Trial sponsor Primary endpoint in a Phase 3 trial

Not on this page

Checked, with nothing recorded for this organization: companies grouped under this page, related companies not grouped here, fda warning letters, fda untitled letters, fda recalls, fda import refusals, manufacturing and distribution sites, organization relationships, clia clinical laboratory certificates, and biomarkers this organization publishes on.