Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Tiziana Life Sciences LTD
Age
18–75
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Adults ≥18 years of age and ≤75 years of age with a diagnosis of symptomatic ALS by revised El Escorial Criteria (clinically possible, probable, probable lab-supported, or definite).
Participant must be actively enrolled and must have met eligibility criteria for the Healey ALS MyMatch Common Screening Protocol (MCSP) AND determined to have met preliminary eligibility on targeted medical history and review of systems and safety laboratory results required for this trial.
Blood neurofilament (NfL) level of greater than 40 pg/mL as measured by the MyMatch Common Screening Protocol specific NfL assay.
Ability to provide written informed consent.
Less than or equal to 24-months since onset of weakness or spasticity attributed to ALS.
Slow vital capacity (SVC) of at least 65% predicted value for gender, height and age at trial screening visit.
Participant must not have taken riluzole and/or edaravone for at least 30 days, or be on a stable dose of riluzole and/or edaravone for at least 30 days prior to baseline (riluzole-naïve or edaravone-naïve participants are permitted in the study).
Negative urine pregnancy test within 7 days prior to the first dose of study therapy for women of child-bearing potential, defined as a sexually mature woman who has not undergone a hysterectomy or who has not been naturally postmenopausal for at least 24 consecutive months (i.e., who has had menses any time in the preceding 24 consecutive months). Sexually active women of child-bearing potential and male participants must agree to use highly effective methods to avoid pregnancy (oral, injectable, or implantable hormonal contraceptive; tubal ligation; intra-uterine device; barrier contraceptive with spermicide; or vasectomized partner) throughout the study and for 90 days after the completion of study treatment.
Participants must be able to travel to the study site for study visits and complete required study procedures.
Participants who are participating in the PET or Lumbar Puncture (LP) outcomes, must be determined to be able to safely tolerate these study procedure(s) in the opinion of the study investigator AND as determined by the targeted medical history and review of systems in the MCSP. Both procedures are highly encouraged.
Participants whose immunizations are fully up to date at Screening, according to the assessment of their primary care physician and neurologist.
You may not be if
Clinically significant medical condition that would pose a risk to the participant, according to the PI's judgment and examination prior to baseline.
Active ENT disease (such as allergic rhinitis, chronic rhinitis, active sinusitis treated within the past 30 days or deemed as clinically relevant, clinically significant deviated nasal septum, nasal polyps) that might interfere with safely administering the drug nasally.
Active clinically significant infection or immunocompromised condition.
Treatment with chronic immunosuppressants or other immunosuppressants within the past 90 days.
Concomitant use of investigational treatments for ALS within 5 half-lives or 30 days prior to the Baseline visit, whichever is longest (high dosage methylcobalamin permitted).
Exposure to any gene or cell therapies under investigation for treatment of ALS.
Inability to tolerate nasally administered medications.
Participant reported history of any vaccines within past 14 days (prior to first dose of foralumab).
Clareo Health | The BANYAN Trial, an ALS MyMatch Trial Evaluating Safety, Biomarker Activity, and Microglial Activation of Nasal Foralumab
