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NCT02839915Active, not recruitingPhase 2

Leucovorin for the Treatment of Language Impairment in Children With Autism Spectrum Disorder

Source: ClinicalTrials.gov · Last updated 27 Apr 2026

Brief summary (registry, in English)

The purpose of this study is to determine the effectiveness of folinic acid in the treatment of language problems in children with autism spectrum disorder. Folinic acid, also known as leucovorin, is approved by the U.S. Food and Drug Administration (FDA) to decrease side effects during cancer chemotherapy. Folinic acid may be helpful in treating language problems in children with autism spectrum disorder, but this is not known. Therefore, folinic acid is an investigational new drug for this study. Investigators will enroll a total of 134 participants across all three centers, over a 5 year period and participation will last between 12 and 24 weeks.

Status (registry)
Active, not recruiting
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
56 (actual)
First submitted
19 Jul 2016
Start date
13 Aug 2020
Primary completion date
15 Apr 2024
Lead sponsor
Southwest Autism Research & Resource Center
Diseases
Autism
NCT number
NCT02839915

What you commit to

  • Study type: Interventional · Phase 2
  • Participants enrolled: 56
  • From 13 Aug 2020 to the primary completion date, 15 Apr 2024
  • 4 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Children taking Bactrim (trimethoprim + sulfamethoxazole) because Bactrim can interfere with folate metabolism. Children who discontinue use of Bactrim for 2 months may be re-evaluated for the study. Caregivers will be advised not to use any of these medications during the trial.
  • Children taking valproic acid or derivatives or lamotrigine for any purpose will be excluded because these drugs can interfere with folate metabolism. Caregivers will be advised not to use any of these medications during the trial.

Other illness

  • Current DSM-IV diagnosis requiring alternative pharmacotherapy, e.g., Major Depression, Bipolar Disorder, a psychotic disorder (based on clinical assessment assisted by the Child and Adolescent Symptom Inventory);
  • Significant medical condition by history or by physical examination or lab tests that would be incompatible with the study drug.
  • Children taking anticonvulsant medication for seizures.

Age

  • IQ below 40 as measured by the Leiter-3 or below a mental age of 18 months on the Receptive Language Scale of Mullen. (N.B. subjects who test below 18 months of age, but are otherwise eligible, may be enrolled following a case review by the Steering Committee - e.g., child's uncooperative behavior resulted in a likely underestimate of intellectual ability);

Other

  • Is within the scorable range of the CELF-4 or CELF-P as detailed in the Language Algorithm;
  • Presence of serious behavioral problems (tantrums, aggression, self-injury) for which another treatment is warranted.
  • Children on mineral or vitamin supplements that exceed the Recommended Daily Allowance set by the IOM.

Who the study is looking for

  • Boys and girls ≥ 5 years and \< 17 years 5 months of age;
  • Weight ≥ 15 kg;
  • DSM-5 diagnosis of Autism Spectrum Disorder as established by clinical assessment, corroborated by the Social Communication Questionnaire and the Autism Diagnostic Observational Schedule.
  • A score \< 80 on the Core Language score of the Clinical Evaluation of Language Fundamentals -4 (CELF)- 4 or the Second Edition of the CELF-Preschool test (CELF-P).
  • Current Clinical Global Impression Severity score ≥ 4 on ASD + communication delay.
  • IQ at least 40 as measured by the Leiter-3 or mental age at least 18 months as measured on the Receptive Language Scale of the Mullen.
  • Stable educational plan (one month) with no planned changes in the intensity of treatment for 12 weeks. (Otherwise eligible subjects with anticipated changes in their school program in the near term will be invited to return when the transition has been accomplished.
  • Stable speech therapy program in the community (one month) with no planned changes for 12 weeks.
  • English is spoken in the home and at least one parent is able to read, write and speak English.
  • Stable medication (no changes in past 6 weeks and no planned changes for the next 6 months (duration of the study).

Age in the registry: 5 years to 17 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (4)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Children's Healtcare of Atlanta
Coordinator of this site? Confirm its status
AtlantaUnited StatesUnknown status
State University of New York, Downstate
Coordinator of this site? Confirm its status
BrooklynUnited StatesUnknown status
Harvard University
Coordinator of this site? Confirm its status
LexingtonUnited StatesUnknown status
Southwestern Research and Resource Center
Coordinator of this site? Confirm its status
PhoenixUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.