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This trial is complete. It is no longer accepting participants.

NCT00004665

NCT00004665
Completed Phase 2

Who may be able to join

Who might be able to join this trial:

  • You have been diagnosed with systemic lupus erythematosus (lupus) based on recognised medical criteria
  • Your lupus is considered mild to moderate
  • You are currently taking prednisone (or a similar steroid) at a dose between 10 and 30 mg per day
  • Either you tried to reduce your prednisone dose in the last 12 months but were unable to, and your dose has been stable for at least 6 weeks — OR you have not tried to reduce your dose in the last 12 months and your dose has been stable for at least 3 months
  • You have previously completed a study involving a supplement called DHEA (dehydroepiandrosterone)
  • You are a woman aged 18 or older
  • If you are able to become pregnant, you have a negative pregnancy test within 2 weeks before joining, and you are using reliable contraception

Who may not be able to join:

  • You previously took part in a double-blind DHEA study at Stanford University
  • You are currently taking immune-suppressing medications
  • You are currently taking part in another clinical study
  • You have taken any experimental treatment within the last 30 days (or longer, depending on the specific medication) (confirm with trial site)
  • You have taken certain immune-suppressing drugs — including cyclophosphamide, azathioprine, or intravenous immunoglobulin — within the last 3 months
  • You have changed your dose of anti-inflammatory drugs (such as ibuprofen) or hydroxychloroquine within the last month
  • You have a known allergy or sensitivity to DHEA, cornstarch, lactose, or magnesium stearate
  • You have any condition that would make it difficult for you to follow the study requirements
  • You have a history of breast cancer or cancer of the reproductive organs
  • You are using an oral contraceptive that contains oestrogen
  • You are male

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.

Phase 2: approximately ~30% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.

Trial details

Status
Completed
Phase
Phase 2
Sponsor
National Center for Research Resources (NCRR)
Registry
clinicaltrials_gov
Start date
1 June 1995

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: 30 June 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

View original record on ClinicalTrials.gov