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Idiopathic HypersomniaPhase 2/3NCT07646678

A Study of TAK-360 in People With Narcolepsy or Idiopathic Hypersomnia

A Phase 2/3 study testing TAK-360 in people with Idiopathic Hypersomnia and Narcolepsy Type 1, run by Takeda at 33 sites in 5 countries.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
Search all trials

Trial summary

Central hypersomnia conditions are a group of sleeping disorders where the brain has trouble keeping a person awake during the day (called excessive daytime sleepiness or EDS). These conditions usually include narcolepsy (type 1 and 2) and idiopathic hypersomnia (IH). Read more about this study

Who is it for?
Ages 18 to 71 years
What is being tested?
TAK-360
Type of treatment
Pill or oral medicine
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
500 participants
Where
33 sitesin 5 countries
Study dates
11 Jun 2026to 15 Jun 2031
Phase
Phase 2/3
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 71 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Participant is willing and able to understand and fully comply with trial procedures and requirements.
  • Participant has a confirmed diagnosis of either NT1, NT2, or IH, and has completed the treatment period of a parent TAK-360 trial.
  • Participant has provided informed consent (that is, in writing, documented via a signed and dated informed consent form (ICF) and any required privacy authorization before the initiation of any trial procedures.

Who cannot join

  • Participant has a positive pregnancy test or is lactating/breastfeeding.
  • Participant has a risk of suicide according to endorsement of item 4 or 5 on the Columbia Suicide Severity Rating Scale (C-SSRS).
  • The participant has developed a new medical disorder associated with excessive daytime sleep (EDS).
  • Participant has developed (within the last 6 months) gastrointestinal disease that is expected to influence the absorption of drugs.
  • Participant has developed a new history of seizures.
  • Participant has experienced clinically significant head injury, per investigator opinion.
Show all 10Show fewer
  • Participant has developed a history of cerebral ischemia, transient ischemic attack (less than [<] 5 years ago), or cerebral haemorrhage.
  • Participant has developed a history of myocardial infarction, clinically significant coronary artery disease, clinically significant angina, clinically significant cardiac rhythm abnormality, or heart failure.
  • The participant has been diagnosed with medically significant thyroid disease, known functional hepatic impairment, or other severe chronic medical condition other than the central hypersomnolence disorder.
  • Participant has developed a history of cancer in the past 5 years.

Trial locations and contacts

33 sites in 5 countries. Contact the study team or a site near you to ask about taking part.

33 sites in 5 countries

United States22 sites, 22 recruiting
  • Takeda Site 6

    Atlanta, Georgia, 30328

    Recruiting
  • Takeda Site 20

    Austin, Texas, 78731

    Recruiting
  • Takeda Site 32

    Bowie, Maryland, 20715

    Recruiting
  • Takeda Site 11

    Brandon, Florida, 33511

    Recruiting
  • Takeda Site 23

    Chula Vista, California, 91910

    Recruiting
  • Takeda Site 2

    Cincinnati, Ohio, 45245

    Recruiting
  • Takeda Site 4

    Cincinnati, Ohio, 45245

    Recruiting
  • Takeda Site 14

    Colorado Springs, Colorado, 80918

    Recruiting
  • Takeda Site 8

    Columbia, South Carolina, 29021

    Recruiting
  • Takeda Site 24

    Denver, North Carolina, 28037

    Recruiting
  • Takeda Site 10

    Huntersville, North Carolina, 28078

    Recruiting
  • Takeda Site 31

    Lansing, Michigan, 48911

    Recruiting
  • Takeda Site 30

    Miami, Florida, 33155

    Recruiting
  • Takeda Site 7

    Miami, Florida, 33176

    Recruiting
  • Takeda Site 19

    Middletown, New Jersey, 07748

    Recruiting
  • Takeda Site 33

    Norfolk, Virginia, 23507

    Recruiting
  • Takeda Site 3

    San Antonio, Texas, 78229

    Recruiting
  • Takeda Site 25

    Santa Ana, California, 92705

    Recruiting
  • Takeda Site 21

    Southfield, Michigan, 48075

    Recruiting
  • Takeda Site 9

    St Louis, Missouri, 63123

    Recruiting
  • Takeda Site 22

    Winston-Salem, North Carolina, 27103

    Recruiting
  • Takeda Site 18

    Winter Park, Florida, 32789

    Recruiting

Other trials in United States

Japan6 sites, 6 recruiting
  • Takeda Site 29

    Isahaya-shi, Nagasaki, 854-0081

    Recruiting
  • Takeda Site 13

    Kumamoto, Kumamoto, 162-0851

    Recruiting
  • Takeda Site 26

    Osaka, Osaka, 532-0003

    Recruiting
  • Takeda Site 1

    Shinjuku-ku, Tokyo, 162-0851

    Recruiting
  • Takeda Site 28

    Urasoe, Okinawa, 901-2132

    Recruiting
  • Takeda Site 27

    Yokohama, Kanagawa, 222-0033

    Recruiting

Other trials in Japan

China3 sites, 3 recruiting
  • Takeda Site 5

    Guangzhou, Guangdong, 510515

    Recruiting
  • Takeda Site 12

    Xicheng, Beijing Municipality, 100053

    Recruiting
  • Takeda Site 16

    Zhenzhou, Henan, 450003

    Recruiting

Other trials in China

Australia1 site, 1 recruiting
  • Takeda Site 15

    Macquarie Park, New South Wales, 2113

    Recruiting

Other trials in Australia

South Korea1 site, 1 recruiting
  • Takeda Site 17

    Daegu, Daegu Gwang'yeogsi, 42601

    Recruiting

Other trials in South Korea

About this study

Official title: A Long-term Extension Trial to Evaluate the Safety and Tolerability of TAK-360 in Participants With Selected Central Hypersomnia Conditions

Central hypersomnia conditions are a group of sleeping disorders where the brain has trouble keeping a person awake during the day (called excessive daytime sleepiness or EDS). These conditions usually include narcolepsy (type 1 and 2) and idiopathic hypersomnia (IH). Narcolepsy type 1 (NT1) includes sudden muscle weakness while you stay awake, called cataplexy, often triggered by strong emotions. Narcolepsy type 2 (NT2) does not include cataplexy. People with narcolepsy typically feel refreshed by short naps. People with IH feel extremely sleepy during the day, and do not feel refreshed by sleep. Waking up from sleep is difficult. This is common in the morning and also when waking up from long naps.

The study wants to learn about TAK-360 when taken over a long time period; this is called a long-term extension or LTE study. The main aim of this LTE study is to find out how well participants with NT1, NT2, and IH tolerate TAK-360 over a longer period (long-term tolerability) and to learn how safe TAK-360 is when given over a longer period of time (long-term safety).

Read more

Participants who completed one of the TAK-360 parent studies can join this study if they meet the study rules. Parent studies include TAK-360-2001(NCT06952699), TAK-360-2002 (NCT06812078), or other TAK-360 studies that evaluate the TAK-360 medicine. All participants will receive TAK-360 in this study. They will either receive the same dose as they did in the parent study, or the closest dose available in this LTE study. Participants who received placebo (the placebo looks just like TAK-360 but does not have any medicine in it) in their parent study will receive one of the TAK-360 doses available in this study. Placebo will only be used to not reveal the dose of TAK-360 from parent studies to investigator, participants, and sponsor. Sponsor, investigators and participants will not know which TAK-360 dose was used in the LTE study as long as the parent study is ongoing.

The participants will have to visit the clinic multiple times during this study.

Being tested
TAK-360, Placebo
Keywords
Drug Therapy
Medical subject headings
Idiopathic Hypersomnia

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • TAK-360Drug

    TAK-360 tablets

  • PlaceboDrug

    TAK-360-matching placebo tablets

Study groups in NCT07646678
Study groupRoleWhat they receive
TAK-360 Long Term Extension (LTE) PhaseExperimentalParticipants will receive one of the available TAK-360 doses for up to approximately 5 years in this trial. Participants will enter the LTE on the dose they were in the parent trial or for participants with discontinued dosing regimen in the parent trial to the next closest available dose/dosing regimen for their indication in this trial. Participants rolling over to this trial from a placebo arm in the parent trial, will receive one of the available TAK-360 doses. Placebo will be only administered as needed to maintain dose blinding between TAK-360 doses and regimens.
Receives: Drug: TAK-360; Drug: Placebo

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Number of Participants With at Least 1 Treatment-Emergent Adverse Event (TEAE)

    An adverse event (AE) is any untoward medical occurrence in a clinical investigation participant administered a pharmaceutical product. A TEAE is defined as any event emerging or manifesting at or after the initiation of treatment with a study intervention or medicinal product or any existing event that worsens in either intensity or frequency following exposure to the study intervention or medicinal product.

    Measured: Up to approximately 5 years

Secondary outcomes (6)
  1. All Participants: Change From Baseline in Epworth Sleepiness Scale (ESS) Total Score

    The ESS provides individuals with 8 different situations of daily life and asks them how likely they are to fall asleep in those situations (scored 0 to 3) and to try to imagine their likelihood of dozing even if they have not actually been in the identical situation; the scores are summed to give an overall score of 0 to 24. Higher scores indicate stronger subjective daytime sleepiness, and scores below 10 are considered to be within the normal range.

    Measured: Baseline through Year 5

  2. All Participants: Change from Baseline in Mean Sleep Latency on the Maintenance of Wakefulness Test (MWT)

    The MWT evaluates a participant's ability to remain awake under soporific conditions for a defined period. Because there is no biological measure of wakefulness, wakefulness is measured indirectly by the inability or delayed tendency to fall asleep. This tendency to fall asleep is measured via electroencephalography-derived sleep latency in the MWT. One MWT, that includes four 40-minute wake trials, will be done. Sleep latency in each wake trial will be recorded. Participants will be required to stay awake in between the 4 MWT wake trials.

    Measured: Baseline through Month 6

  3. IH Participants: Change From Baseline in IH Severity Scale (IHSS) Total Score

    The IHSS is a 14-item self-assessment questionnaire, to measure the severity, frequency and functional impact of the 3 key IH symptoms (during a recall period of "past 7 days"). The IHSS includes 2 items (1 and 2) on nighttime sleep duration and quality, 3 items (3, 4, and 5) on sleep inertia and sleep drunkenness after nighttime sleep and 1 (8) after daytime nap, and 3 items (6, 7, and 9) on diurnal symptoms (nap occurrence, daytime sleepiness). Items 10 to 14 assess daytime functioning alterations due to hypersomnolence. Six items (1,2,3,5,7,8) are scored with 4 ranged response options, with score from 0 to 3, and 8 items (4,6,9,10,11,12,13,14) with 5 ranged response options, with score from 0 to 4, with 1 additional response option for item 14. The total IHSS score is the sum of all item scores (range: 0 to 50); higher scores indicate more severe symptoms.

    Measured: Baseline through Year 5

  4. NT1 Participants: Change From Baseline on the Narcolepsy Severity Scale for Clinical Trials (NSS-CT)

    The NSS-CT is a 15-item self-administered questionnaire that assesses the severity and consequences of the 5 major narcolepsy symptoms such as daytime sleepiness, cataplexy, hallucinations, sleep paralysis, and disrupted nighttime sleep (DNS) with a total score range of 0 to 57 (sum of 8 items that assess symptoms severity [2 with 4 response options, 1 response with 6 options, and 5 items capturing event count], and 7 items that describe the symptom effect on daily life with 4 response options). The presence of narcolepsy symptoms is defined by EDS (score greater than or equal to [≥] 1 on at least one of items 1, 2, 3, 4, 5, 6, or 7), cataplexy (score ≥1 on at least one of items 8, 9, or 10), hallucinations (score ≥1 on at least one of items 11 and 12), sleep paralysis (score ≥1 on at least one of the items 13 and 14), and disrupted nighttime sleep by a score ≥1 on item 15. Higher scores indicate greater symptom severity or degree of impact.

    Measured: Baseline through Year 5

  5. NT2 Participants: Change From Baseline on the Narcolepsy Severity Scale for Clinical Trials (NSS-2-CT)

    The NSS-2-CT is a 12-item self-administered questionnaire that assesses the severity and consequences of major narcolepsy symptoms such as daytime sleepiness, hallucinations, sleep paralysis, and disrupted nighttime sleep, with higher scores indicating more severe narcolepsy symptoms and impacts. The total score ranges from 0-44(sum of 6 items that assess event symptom severity [including 2 items with 4 response options, 1 item with 6 response options, and 3 items capturing event count], and 6 items that describe symptom effect on daily life, with 4 response options), and differs from the NSS-CT in its omission of cataplexy-related items. The presence of narcolepsy symptoms is defined by EDS (score ≥1 on at least one of items 1, 2, 3, 4, 5, 6, or 7), hallucinations (score ≥1 on at least one of items 8 and 9), sleep paralysis (score ≥1 on at least one of the items 10 and 11), and disrupted nighttime sleep by a score ≥1 on item 12.

    Measured: Baseline, Month 1 through Year 5

  6. Change from Baseline in Weekly Cataplexy Rate (WCR) Using the Participant-Reported Cataplexy eDiary

    Participants will complete a patient-reported sleep diary to record self-reported narcolepsy symptoms. Participants will record episodes of cataplexy attacks in the diary. The total number of events averaged for a week will be reported.

    Measured: Baseline, Month 3 through Month 24

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted15 Jun 2026
  2. Study start11 Jun 2026
  3. Primary completion15 Jun 2031 (estimated)
  4. Study completion15 Jun 2031 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 2/3
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
500 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07646678
Sponsor's protocol ID
TAK-360-2003
Other IDs
2025-522833-68-01, jRCT2031260198, 2025
Status last verified
Nov 2026
First submitted
9 Jun 2026
Last updated
5 Nov 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
Yes
FDA-regulated device
No
Individual data sharing
Yes: Takeda provides access to the de-identified individual participant data (IPD) for eligible studies to aid qualified researchers in addressing legitimate scientific objectives (Takeda's data sharing commitment is available on https://clinicaltrials.takeda.com/takedas-commitment?commitment=5). These IPDs will be provided in a secure research environment following approval of a data sharing request, and under the terms of a data sharing agreement.

Questions about this trial

What is this clinical trial studying?

A Phase 2/3 study testing TAK-360 in people with Idiopathic Hypersomnia and Narcolepsy Type 1, run by Takeda at 33 sites in 5 countries.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 10 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 5 Nov 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 33 sites in United States, Japan, China, Australia, South Korea. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this combined phase mean?

Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.

Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Study Director (+1-877-825-3327, medinfoUS@takeda.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Number of Participants With at Least 1 Treatment-Emergent Adverse Event (TEAE) (time frame: Up to approximately 5 years). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 5 Nov 2026.

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