A Study to Evaluate the Safety and Efficacy of CD388 for Prevention of Influenza

Running, not enrolling · Phase 3 · Has a placebo group

Conditions studied: Influenza

In brief

The purpose of this study is to evaluate how well CD388 works in preventing symptomatic laboratory-confirmed influenza infections, as compared to placebo, when given as a single dose via 3 subcutaneous (SQ) injections to adult and adolescent participants who are at higher risk of developing influenza complications, and to evaluate the safety and tolerability of CD388, as compared to placebo.

Key facts

Study ID

NCT07159763

Run by

Cidara Therapeutics Inc., a subsidiary of Merck & Co., Inc. (Rahway, New Jersey USA)

People needed

10000

Starts

2025-09-25

Expected to finish

2027-06-01

Last updated by the study team

2026-06-22

Who can join

Age: 12 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Must be 12 years of age or older at the time of signing the informed consent.
• Written informed consent and any locally required authorization (e.g., Health Insurance Portability and Accountability Act [HIPAA] in the US) obtained from the participant before performing any protocol-related procedures, including screening evaluations. For participants under the legal age of consent as defined by local regulations, the parent(s) or legal guardian(s) may be required to give their signed written informed consent and participants may sign an assent form as specified by local law.
• Has negative rapid antigen tests for influenza and severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) prior to dosing at Day 1.
• Weight is ≥ 40 kilograms (kg) at screening.
• Body Mass Index (BMI; calculated as weight in kg divided by height in meters [m] squared)) is ≥ 18 kg/m\^2 at screening.
• In the opinion of the Investigator or designee, must be able to comply with the requirements of the protocol and be able to read, understand, and complete questionnaires in the electronic diary (eDiary), work with smartphones/tablets/computers (if applicable, with assistance by a caregiver, surrogate, or legally authorized representative), and be willing and able to adhere to the prohibitions and restrictions specified in this protocol. If an appropriate language version is not available for the eDiary assessments, the participant should not be enrolled.
• Must be assessed by the Investigator or designee as medically stable and not requiring significant change in maintenance therapy and has not been hospitalized for worsening disease or any significant medical event during the 2 months before screening
• Female participants must agree to the following contraception requirements:
• a. Females of childbearing potential must use a highly effective, preferably user-independent, method of contraception (failure rate of less than 1 percent per year when used consistently and correctly) from ≥2 weeks prior to randomization and agree to remain on a highly effective method from Day 1 until 32 weeks after study intervention administration, the end of relevant systemic exposure. Note: A woman is considered of childbearing potential (i.e., fertile) following menarche and until becoming postmenopausal, unless permanently sterile. Permanent sterilization methods include hysterectomy, bilateral salpingectomy, and bilateral oophorectomy. A postmenopausal state is defined as no menses for 12 months without an alternative medical cause. A high follicle stimulating hormone (FSH) level in the postmenopausal range may be used to confirm a postmenopausal state in women not using hormonal contraception or hormonal replacement therapy. However, in the absence of 12 months of amenorrhea, a single FSH measurement is insufficient.
• Note: Contraceptive (birth control) use by participants should be consistent with local regulations regarding the acceptable methods of contraception for those participating in clinical studies.
• Must agree not to donate blood or blood products from Day 1 until 32 weeks after study intervention administration.
• Must be willing to provide verifiable identification, has means to be contacted, and is able to contact the Investigator or designee/study site and communicate reliably during participation in the study.
• In addition to inclusion criteria 1 through 10 above, participants are eligible to be included in Primary Stratum A of the study (higher risk non-immunocompromised) only if one or more of the following criteria apply:
• Has a history of pulmonary disease; specifically:
• Chronic obstructive pulmonary disease (COPD), including chronic bronchitis and emphysema, graded as follows using the Global Initiative for Chronic Obstructive Lung Disease (GOLD) Categories A, B, and E (ABE) (i.e., GOLD ABE) assessment tool:
• Gold Grade 2 (moderate) or Grade 3 (severe) with following exacerbation history, within 1 year of screening
• At least 2 moderate exacerbations (i.e., not leading to hospitalization), or
• At least 1 exacerbation leading to hospitalization OR
• Gold Grade 4 regardless of exacerbation history
• Bronchiectasis, cystic fibrosis, interstitial lung disease, pneumoconiosis, or past or active bronchopulmonary dysplasia.
• Has moderate to severe asthma, as defined by the Global Initiative for Asthma (GINA) Treatment Steps 3-5.
• Has existing cardiac disease; specifically:
• Congenital heart disease
• Congestive heart failure New York Heart Association (NYHA) Class II-IV
• Coronary artery disease requiring regular medication and/or follow-up for ischemic heart disease (i.e., participants who, through interventional procedure[s] and/or active medical treatment, have attained an established state of chronic stability of a duration of no less than 6 months)

You may not qualify if…

• A female who is pregnant or lactating.
• Known or suspected allergy or history of anaphylaxis or other serious adverse reactions to zanamivir (following administration of inhaled or intravenous formulations), monoclonal antibodies (including crystallizable fragment [Fc] domains), or any of the components of CD388 or placebo.
• Has been diagnosed with influenza (i.e., with medical history [including verbal] of influenza) within 6 months prior to randomization.
• Has received the current seasonal inactivated influenza vaccine or live attenuated influenza vaccine within the 14 days prior to dosing on Day 1. (NOTE: Participant may have received recombinant influenza vaccine up to the day of dosing on Day 1.)
• Has an acute (time-limited) or febrile (temperature ≥38.0 degrees Celsius [ºC] [≥100.4 degrees Fahrenheit {ºF}]) illness within 7 days prior to planned dosing on Day 1.
• Has had close contact (including household contact) with someone with laboratory-confirmed influenza or SARS-CoV-2 or with someone who has been treated with antiviral therapies for influenza or SARS-CoV-2 within the 7 days prior to randomization.
• Has a clinically unstable condition including, but not limited to, a psychiatric condition, including recent (within the past year) or active suicidal ideation/behavior, or any other condition for which, in the opinion of the Investigator or designee, may lead to hospitalization or death within the study period and that suggests that study enrollment would not be in the participant's best interest and/or that could prevent, confound, or limit the protocol-specified assessments.
• Has any history of alcohol or drug abuse that, in the opinion of the Investigator or designee, would adversely impact the conduct of the study.
• Had major surgery (e.g., major cardiac, pulmonary or abdominal operation) within 4 weeks prior to randomization, or will not have fully recovered from surgery, or has major surgery planned during the time the participant is expected to participate in the study.
• Has severe CKD (equivalent to an eGFR less than 30 mL/min/1.73 m\^2 as calculated by CKD-EPI equation for adults or the CKiD U25 equation for adolescents), or is receiving hemodialysis.
• Has screening electrocardiogram (ECG) findings of prolonged QT interval corrected using Fridericia's formula (QTcF) (greater than 450 milliseconds [msec] in males or greater than 470 msec in females), prolonged PR interval (greater than 220 msec), second- or third-degree heart block, or other clinically significant dysrhythmias, unless participant has a known cardiac diagnosis responsible for the ECG findings and is in stable condition. NOTE: Participants with cardiac pacemakers may be enrolled if no exclusion criteria are met.
• Current or planned participation in another clinical study in which study intervention is being administered during participation in the current study. NOTE: Concurrent enrollment is allowed during the follow-up phase of the other clinical study or in case the study intervention in the other clinical study is a marketed product already approved for another indication - exception being if the other study requires study interventions that could affect the safety assessments of the present study (e.g., clinical laboratory tests).
• Receipt within the past 30 days or 5 half-lives (whichever is longer) or anticipated receipt of any drug or other biologic agent (e.g., monoclonal antibodies) administered for the prevention or treatment of influenza.
• Receipt of any formulation of immunoglobulin within 14 days prior to planned study intervention administration.
• Receipt of any experimental drug, vaccine, or biologic agent within the 90 days or 5 half-lives (whichever is longer) prior to study intervention administration.
• Has a clinically significant bleeding disorder (e.g., factor deficiency, coagulopathy, or platelet disorder) or medical history of significant bleeding or bruising following intramuscular or SQ injections or venipuncture. NOTE: Participants receiving apixaban or warfarin may be enrolled if the Investigator or designee determines risk of SQ treatment with study intervention on Day 1 is minimal.
• Has donated ≥450 mL of blood product (1 unit) for any reason within 30 days of screening.
• Has direct involvement in the proposed study or other studies under the direction of the Investigator or designee, sub-investigators, or at the study site; or is a family member of an individual with such direct involvement; or is an employee of the Sponsor; or was previously enrolled and dosed in a CD388 clinical trial.
• In the Investigator's or designee's judgment, the participant has any condition or circumstance present that significantly increases risk, affects the ability to participate, impairs interpretation of study data, or indicates a likelihood of non-adherence to study requirements.
• Has previously enrolled in this study (CD388.SQ.3.06).

Where it is running

• Cullman Clinical Trials — Cullman, Alabama, United States
• HOPE Research Institute — Glendale, Arizona, United States
• Desert Clinical Research, LLC / Avacare — Mesa, Arizona, United States
• Foothills Research Center / Avacare — Phoenix, Arizona, United States
• Fiel Family and Sports Medicine / Avacare — Tempe, Arizona, United States
• HOPE Research Institute — Tempe, Arizona, United States
• Arizona Clinical Trials — Tucson, Arizona, United States
• Del Sol Research Management, LLC — Tucson, Arizona, United States
• Triallogix Medical Corporation — Fullerton, California, United States
• National Institute of Clinical Research, Inc. — Garden Grove, California, United States
• Eximia Research-CA, LLC — La Mesa, California, United States
• Kinetic Clinical Research, LLC dba Long Beach Clinical Trials — Long Beach, California, United States
• Seaside Medical Group — Oceanside, California, United States
• Profound Research, LLC — Pasadena, California, United States
• Paradigm Clinical Research — Redding, California, United States
• Artemis Institute for Clinical Research — San Diego, California, United States
• Acclaim Clinical Research — San Diego, California, United States
• Diablo Clinical Research, Inc. — Walnut Creek, California, United States
• Tekton Research, LLC — Denver, Colorado, United States
• Tekton Research, LLC — Fort Collins, Colorado, United States
• Critical Care, Pulmonary and Sleep Associates PLLP / Avacare — Lakewood, Colorado, United States
• Tekton Research, LLC — Longmont, Colorado, United States
• New England Research Associates — Bridgeport, Connecticut, United States
• Stamford Therapeutics Consortium — Stamford, Connecticut, United States
• Pinnacle Research Group, LLC — Anniston, Alabama, United States

Full record on ClinicalTrials.gov

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