Early Phase 1 Parkinson's Disease Trial, Recruiting NCT07617688 Sponsor: MODAG GmbH Condition: Parkinson's Disease
Back to Parkinsons Disease

Early Phase 1 Parkinson's Disease Trial, Recruiting

NCT07617688
Recruiting Early Phase 1

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • People aged 18 to 60 years old
  • People who are generally in good health, as confirmed by a physical check-up, blood tests, heart trace (ECG), and review of medical history at the screening visit
  • People who are able to follow all study procedures as required
  • People who are able to read, understand, and sign a consent form agreeing to take part
  • Women who are not able to become pregnant — either because they have gone through menopause (no periods for at least 12 months) or have had a surgical procedure such as removal of the ovaries, fallopian tube ligation, or hysterectomy
  • Women who are able to become pregnant but are using a highly effective form of contraception (such as the oral contraceptive pill taken for at least 3 months beforehand, an IUD fitted at least 2 months beforehand, or a barrier method such as a diaphragm or condom with spermicide) starting at least 14 days before the study injection and for at least 24 hours after — note that periodic abstinence methods (such as calendar or ovulation tracking) are not accepted under the trial criteria
  • Men whose female partners could become pregnant must use adequate contraception and must not donate sperm for 90 days after the study injection

Who may not be able to join:

  • People who have taken prescription medications or herbal supplements within 4 weeks before the first dose, or over-the-counter medications or dietary supplements (including vitamins) within 2 weeks before the first dose (limited use of paracetamol/acetaminophen may be acceptable — confirm with trial site)
  • People who have taken part in another clinical trial within 4 weeks before the first dose, or within 5 half-lives of the investigational drug used in that trial if that period is longer than 4 weeks
  • People who have been exposed to more than 50 millisieverts (mSv) of radiation in the past year — for example, through work or radiation treatment
  • People who have donated or lost 400 ml or more of blood within 8 weeks before the first dose (or longer if required by local rules)
  • People who have a current or past significant health condition affecting the heart, lungs, liver, kidneys, digestive system, hormonal system, or nervous system that the study doctor believes could affect how the study drug is processed by the body, or that could put the person at risk
  • People with abnormal results on blood or urine laboratory tests that the study doctor considers clinically significant
  • People with significant abnormal findings on a heart trace (ECG)
  • People with a history of immune system diseases, or a positive test result for HIV
  • People who test positive for Hepatitis B or Hepatitis C
  • People with a history of drug or alcohol misuse in the 12 months before screening, or whose screening tests suggest current misuse
  • People who have used tobacco products within 3 months before screening (confirmed by a urine test)
  • Women who have a positive pregnancy test result
  • Women who are currently breastfeeding or lactating

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 28 July 2026
Early Phase 1 studies are small, early exploratory studies that come before the main Phase 1 to 3 testing, so a standard phase success rate does not apply.

Contact this trial

Principal Investigator: Neha Prakash, MBBS, Institute for Neurodegenerative Disorders

Phone: 475-318-8250

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Early Phase 1
Sponsor
MODAG GmbH
Registry
ClinicalTrials.gov
Start date
27 May 2026
Est. completion
1 May 2027

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Safety and Tolerability

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov