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MEMP1972A

Phase 2

Asthma | Small molecule | Respiratory |Roche Holding AG|Last Updated: Dec 12, 2022

Success Probability

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Market & Valuation

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Trial Design

RandomizedDouble-BlindPLACEBO_CONTROLLED
Total Trials2
Total Enrollment607

FDA Designations

No designations recorded

Clinical trial landscape

MEMP1972A · 3 trials · 2 indications

Phase 2 2Phase 1 1
NCT01582503A Study of MEMP1972A in Patients With Allergic Asthma Inadequately Controlled on Inhaled Steroids And A Second Controller (COSTA)Asthma
COMPLETED578 Analytics
NCT01196039A Study of MEMP1972A in the Prevention of Allergen-Induced Airway Obstruction in Patients With Mild Asthma (SOLARIO)Asthma
COMPLETED29 Analytics
PHASE2COMPLETED
A Study of MEMP1972A in Patients With Allergic Asthma Inadequately Controlled on Inhaled Steroids And A Second Controller (COSTA)
AsthmaUnlock trial analytics
PHASE2COMPLETED
A Study of MEMP1972A in the Prevention of Allergen-Induced Airway Obstruction in Patients With Mild Asthma (SOLARIO)
AsthmaUnlock trial analytics

Study Endpoints

Primary Endpoints

Rate of protocol-defined asthma exacerbations (new or increased asthma symptoms that lead to treatment with systemic corticosteroids or to hospitalization) from baseline to Week 36
36 weeks
Late airway response (LAR) area under the concentration-time curve (AUC) (percent decline in forced expiratory volume in 1 second [FEV1] over time)
Between 3 and 7 hours after allergen challenge at Day 86 after the first dose
Incidence and nature of laboratory abnormalities, based on hematology, clinical chemistry, and urinalysis test results
Throughout study or until early discontinuation
Incidence, nature, and severity of adverse events
Throughout study or until early discontinuation

Secondary Endpoints

Relative change in pre-bronchodilator FEV1 (volume)
from baseline to Week 12
Relative change in FEV1 (volume)
from baseline to Week 36
Change in asthma symptoms
from baseline to Week 12
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Study Design & Arms

AllocationRANDOMIZED
MaskingDOUBLE
ModelPARALLEL
PurposeTREATMENT

Treatment Arms

ArmTypeDescription
MEMP1972A 150 mgEXPERIMENTAL -
MEMP1972A 300 mgEXPERIMENTAL -
MEMP1972A 450 mgEXPERIMENTAL -
PlaceboPLACEBO_COMPARATOR -
AEXPERIMENTAL -
BPLACEBO_COMPARATOR -
CEXPERIMENTAL -

Interventions

NameTypeDescription
MEMP1972ADRUGSubcutaneous repeating dose
placeboDRUGSubcutaneous repeating dose
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Eligibility Criteria

Age Range18 Years to 75 Years
SexALL
Healthy VolunteersNo
Study Sites145

Inclusion Criteria: * Adult patients, 18 to 75 years of age inclusive * Body weight \>/= 40 kg * Physician's diagnosis of asthma for at least 12 months * Evidence of documented bronchodilator reversibility as defined by protocol * Prebronchodilator FEV1 \>/= 40% and \</= 80% predicted at Visit 1 * ...

Countries:United StatesArgentinaBelgiumBulgariaCanadaGermanyHungaryMexicoNew ZealandPeruPolandRomaniaRussiaUkraineSweden
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Frequently asked questions about MEMP1972A

What is MEMP1972A used for?

MEMP1972A is an investigational small molecule being developed by Roche Holding AG for the treatment of allergic rhinitis and asthma. It has been studied in clinical trials for these respiratory conditions, including in patients with allergic asthma inadequately controlled on inhaled steroids and a second controller.

What does MEMP1972A target?

MEMP1972A is a small molecule, but its specific molecular target has not been disclosed in the available information. The drug has been investigated for its effects on allergic rhinitis and asthma, suggesting it may modulate pathways involved in allergic airway inflammation.

Who makes MEMP1972A?

MEMP1972A is being developed by Roche Holding AG, which trades under the ticker RHHBY. The company has sponsored clinical trials of this investigational drug for allergic rhinitis and asthma.

What phase is MEMP1972A in?

MEMP1972A has completed Phase 1 and Phase 2 clinical trials. The most advanced studies were Phase 2 trials in asthma patients. However, the drug is still investigational and has not been approved by regulatory authorities.

What clinical trials is MEMP1972A in?

MEMP1972A has been studied in three completed trials: NCT01160861, a Phase 1 safety and pharmacokinetics study in allergic rhinitis patients; NCT01196039 (SOLARIO), a Phase 2 study in mild asthma; and NCT01582503 (COSTA), a Phase 2 study in allergic asthma patients on inhaled steroids and a second controller.

Is MEMP1972A the same as other drugs?

MEMP1972A is not known to have alternative names. It is a distinct investigational compound developed by Roche, and no other names for this drug have been reported in the available clinical trial information.