Healthpoint

25 total trials 22 completed

Healthpoint sponsors 25 registered US clinical trials on ClinicalTrials.gov, none currently recruiting, and 22 completed. 11 of these trials are in Phase 3-4 (later-stage) and 11 in Phase 1-2 (earlier-stage). The most-studied condition in this pipeline is Follow up to Acute Wound Scar Study, with 1 trials.

Trial Pipeline

25 total, page 1 of 1

TERMINATED Phase 2

A Phase 2 Exploratory Pharmacodynamic Study of HP802-247 in Venous Leg Ulcers

NCT02154087

COMPLETED Phase 4

Santyl Applications to Diabetic Foot Ulcers

NCT02111291

COMPLETED Phase 4

Study of Oasis Ultra in Diabetic Foot Ulcers

NCT01835379

COMPLETED Phase 3

Study Investigating the Safety and Efficacy of HP802-247 in the Treatment of Venous Leg Ulcers >12 cm2 to ≤ 36 cm2

NCT01737762

COMPLETED

Long Term Follow Up to Determine the Effects of Collagenase SANTYL Ointment on Scar Formation

NCT01705860

COMPLETED Phase 3

Study Investigating the Safety and Efficacy of HP802-247 in the Treatment of Venous Leg Ulcers

NCT01656889

TERMINATED Phase 2

Comparison of HP011-101 to Standard Care for Stage I-II Pressure Ulcers in Subjects With Spinal Cord Injury

NCT01433159

COMPLETED Phase 4

Using Santyl on Diabetic Foot Ulcers

NCT01408277

COMPLETED Phase 2

Healing Effects of HP802-247 Versus Antibiotic Ointment in Mohs Micrographic Surgery Patients

NCT01359735

COMPLETED Phase 1

Study to Determine if Fibrin Affects the Ability of a Wound to Heal

NCT01253135

COMPLETED Phase 4

Wound Edge Changes Following Treatment With Santyl

NCT01197898

COMPLETED Phase 1

Study of Survival Duration for Donor Skin Cells in Skin Biopsy Wounds

NCT01190865

COMPLETED Phase 4

Enzymatic Versus (vs) Autolytic Debridement of Diabetic Foot Ulcers

NCT01143727

COMPLETED Phase 4

A Study to Look at the Effects of Four Weeks of Treatment on the Healing of Diabetic Foot Ulcers

NCT01143714

TERMINATED Early Phase 1

Evaluation of Effects of HP828-101 for Moisture Associated Skin Damage

NCT01108523

COMPLETED Phase 4

Santyl vs. Sharp Debridement of Diabetic Foot Wounds

NCT01056198

COMPLETED NA

Evaluation of the Effects of HP828-101 Versus Standard of Care in the Management of Partial or Full Thickness Wounds

NCT00971048

COMPLETED

Safety Follow-Up to HP 802-247-09-015

NCT00900029

COMPLETED Phase 2

Dose Finding Study of HP802-247 in Venous Leg Ulcers

NCT00852995

COMPLETED Phase 1

Cumulative Irritation Potential of 828 Ointment

NCT00767455

COMPLETED Phase 1

Contact Sensitization Potential of 828 Ointment

NCT00767676

COMPLETED Phase 2

Controlled Study of the Effect of Xenaderm® Ointment Vehicle Versus White Petrolatum on Healing

NCT00713349

COMPLETED Phase 4

Effect of Collagenase on Healing and Scarring

NCT00651820

COMPLETED Phase 1

Clinical Evaluation of the Photoallergy Potential of Xenaderm Ointment

NCT00645164

COMPLETED Phase 4

OASIS Wound Matrix (Oasis) Mechanism of Action

NCT00570141

Phase Distribution

PhaseTrial count
Phase 1 6
Phase 2 5
Phase 3 2
Phase 4 9

What the Pipeline for Healthpoint Shows

According to the ClinicalTrials.gov registry, Healthpoint is linked to 25 US clinical trials across every stage of research activity. Of those, 0 studies are currently recruiting, about 0% of the sponsor's indexed portfolio, and 22 are already marked complete, representing roughly 88% of the total.

The phase mix for Healthpoint reports 11 late-stage studies (Phase 3 and Phase 4 combined) and 11 earlier-phase studies (Phase 1 and Phase 2).

The top therapeutic focus area indexed for Healthpoint is Follow up to Acute Wound Scar Study with 1 linked trial, and 3 other condition areas appear in the top list above.

How to read these pipeline numbers

Recruiting share is one of the more practical signals here: it reflects how much of a sponsor's research is presently open to new participants, while the completed share indicates the depth of finished work that has already contributed registry results. Both counts come directly from the public ClinicalTrials.gov dataset and are refreshed on the registry side; this page mirrors the latest data pull without altering it.

A portfolio weighted toward Phase 3 usually reflects an organization advancing candidates toward regulatory review, where the research centers on comparative efficacy and broader safety across larger populations. A heavier Phase 1 and Phase 2 tilt generally indicates exploratory work, safety, dosing, and early signal detection, and is common among research-forward sponsors that seed many early programs. Phase 4 entries, when present, track interventions already in real-world use and typically focus on long-term safety, effectiveness across subgroups, or formulation comparisons.

That distribution is a quick read of where the organization concentrates its research attention; it does not imply product availability, market share, or any clinical endorsement. All numbers on this page come from ClinicalTrials.gov maintained by the National Library of Medicine, and counts can shift as new studies are registered or existing ones update their status. This information is provided for reference and educational purposes only, not as medical, investment, or regulatory advice, verify current details directly with ClinicalTrials.gov before relying on any figure here.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page aggregates every registered trial from this sponsor, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.