Zero ad trackers.We never sell your data.

Vanda Pharmaceuticals Inc.

Latest, March 26, 2026On March 26, 2026, the FDA issued its decision on Vanda's request for a hearing on the agency's proposal to refuse approval of tradipitant for gastroparesis. FDA, Federal Register

Vanda Pharmaceuticals Inc. works on 2 rare diseases tracked on Trial Friend, including Gastroparesis, Multiple Sclerosis, with 2 active clinical trials (1 recruiting) and 1 FDA-approved rare disease drug.

Vanda Pharmaceuticals is a Washington, DC drugmaker founded in 2003 that markets Hetlioz (tasimelteon), approved for nighttime sleep problems in Smith-Magenis syndrome as well as non-24-hour sleep-wake disorder, and its other medicines include Fanapt, Ponvory and Nereus, with Bysanti approved in February 2026. In gastroparesis, the FDA declined to approve Vanda's tradipitant in September 2024, and Vanda has challenged that outcome; the FDA later approved tradipitant, as Nereus, to prevent vomiting caused by motion.

Type
Diversified Pharma
Ticker
VNDA
Headquarters
Washington, DC, United States
Founded
2003
2
Active Rare Disease Trials
1
Approved Rare Disease Drugs
2
Rare Diseases in Portfolio
23
Years Active

Vanda Pharmaceuticals Inc. Drug Pipeline

Vanda Pharmaceuticals Inc. has 2 active clinical trials across 2 development stages, with 1 currently recruiting participants. Clinical trials advance through phases: Phase 1 tests safety in a small group, Phase 2 evaluates effectiveness and side effects, Phase 3 confirms benefit in a larger population, and Phase 4 monitors long-term safety after FDA approval.

Note: This pipeline counts the active and recruiting trials listed on this page, from ClinicalTrials.gov. For companies that work outside rare disease, we list only trials for rare diseases we track, so the company's full pipeline may be larger.

Understand Vanda Pharmaceuticals Inc.'s pipeline
Answers with sources, in plain English
Start withor ask
1
Phase 21 trial
Active Not Recruiting
1
Phase 31 trial
Recruiting

Vanda Pharmaceuticals Inc. Clinical Trials (2)

Active and recruiting clinical trials sponsored by Vanda Pharmaceuticals Inc., sourced live from ClinicalTrials.gov. Each trial card shows the study phase, current recruitment status, conditions under investigation, study locations, eligibility criteria, and a direct link to the full ClinicalTrials.gov record. You can also download a one-page PDF summary to share with your doctor.

Note: Recruitment statuses on ClinicalTrials.gov may not immediately reflect recent FDA decisions, sponsor announcements, or enrollment changes. Always confirm a trial's current status directly with the study coordinator.

Ask about Vanda Pharmaceuticals Inc.'s trials
Answers with sources, in plain English
Start withor ask
RECRUITINGPHASE3Hasn't posted an update in over a yearNCT06836557

Open Label Safety Study of Tradipitant in Idiopathic and Diabetic Gastroparesis

Intervention: Tradipitant

This is a multicenter, open label, 3-month safety study with tradipitant in patients with idiopathic and diabetic gastroparesis.

Ages 18 Years - 70 Years3 locations
View full study
ACTIVE NOT RECRUITINGPHASE1, PHASE2Recently updatedNCT07223632

Treatment of Charcot-Marie-Tooth Disease, Axonal, Type 2S (CMT2S) in an Individual Patient

Intervention: VCA-894A

Charcot Marie Tooth Disease (CMT)Neuromuscular Diseases (NMD)

This is an 'N of 1', open-label, single center study to evaluate the safety of therapy with VCA-894A, an ASO designed to rescue and restore the activity of IGHMBP2, when administered by intrathecal injection.

Ages not specified1 location
View full study
Follow a condition Vanda Pharmaceuticals Inc. is studying

Pick a condition. One email when a new trial opens, a trial changes or the FDA decides, from any company, not only Vanda Pharmaceuticals Inc.. Unsubscribe anytime.

You'll get new recruiting trials, changes to trials, FDA decisions and condition news for Gastroparesis. Turn any of these off from the link in every email.

We never share your email. Unsubscribe anytime. Privacy policy · Check any health site

Vanda Pharmaceuticals Inc. FDA-Approved Drugs (1)

Medications developed or marketed by Vanda Pharmaceuticals Inc. that have received U.S. Food and Drug Administration approval. Drug data is sourced from the openFDA database and includes brand names, generic names, approval dates, and matched rare disease indications. Where a drug treats a condition covered by Trial Friend, the disease name links directly to that disease page.

Drug NameBrand NameRare DiseasesApproval Date
PONESIMOD
Sphingosine 1-phosphate Receptor Modulator [EPC]
PONVORY
oral
Mar 18, 2021

Vanda Pharmaceuticals Inc. Trial Locations

Vanda Pharmaceuticals Inc. clinical trials are running at 4 sites in 3 countries. Click any country to drill down by state, city, and individual research facility. Proximity to a trial site is one of the most important factors in deciding whether to participate.

Belgium
2▼
Germany
1▼
United States
1▼

Rare Disease Focus Areas (2)

Diseases targeted by Vanda Pharmaceuticals Inc.'s clinical trial and drug development programs

Patient Resources

Organizations and resources related to Vanda Pharmaceuticals Inc.'s rare disease focus areas

Frequently Asked Questions About Vanda Pharmaceuticals Inc.

Common questions about Vanda Pharmaceuticals Inc.'s rare disease programs, clinical trials, and treatments.