A Study to Evaluate the Safety, Pharmacokinetics, and Occurrence of Anti-Drug Antibodies Following Annual Doses of CD388

NCT07225959 | Active Not Recruiting Phase 2 FDA Drug

• 1 other identifier: CD388.SQ.2.07
• Study Type: interventional
• Target: 400
• Locations: 2 countries
• Sites: 3

Brief Summary

The goal of this clinical study is to learn if giving repeated annual doses of the experimental drug CD388 is safe and how the body reacts to it in healthy adults who have already received one dose without serious side effects. The study aims to determine if the body makes antibodies against CD388 after repeated doses, which might affect how the drug works or how safe it is, and to better understand the safety and tolerability of repeated doses. Participants will receive two doses of CD388 over two years and be monitored for 18 months. Researchers will check for immune responses against the drug, watch for any side effects, and measure how the drug behaves in the body over time. This study is based on the idea that people who tolerated CD388 well before will likely continue to tolerate it safely with repeated annual dosing, and that the risk of immune reactions will remain low. Expanded access to the study drug will not be provided to participants after the study ends.

Conditions

Healthy Participants

Keywords

Influenza; Antiviral Agents

Outcome Measures

Primary Outcomes (1)

• Occurrence of Anti-Drug Antibodies (ADAs) in Participants Administered CD388

  Evaluation of blood serum samples for the occurrence of treatment-emergent anti-drug antibodies (ADAs) or treatment-boosted ADAs (based on an increase in ADA titer in samples positive for ADA at baseline) directed to CD388 in participants following administration of each annual dose of CD388.

  On Day 1 (pre-dose baseline), Day 29, Day 85, Day 169, and Day 197 in Study Period 1; on Day 1 (pre-dose), Day 29, Day 85, Day 169, and Day 197/End of Study (EOS) in Study Period 2

Secondary Outcomes (6)

• Incidence and Severity of Treatment-Emergent Adverse Events (TEAEs) after Administration of Study Drug

  From Study Period 1 Day 1 after study drug dosing through Study Period 2 Day 197/EOS

• Plasma Concentrations at Specified Timepoints Following Administration of CD388

  In both Study Periods 1 and 2 on Day 1 (pre-dose), Day 8, Day 29, Day 85, Day 169, and Day 197/EOS as applicable

• Trough Plasma Concentration at 24 Weeks (C[trough24w]) Following Administration of CD388

  In both Study Periods 1 and 2 on Day 169

• Maximum Plasma Concentration (C[max]) Following Administration of CD388

  In both Study Periods 1 and 2 on Day 1 (pre-dose), Day 8, Day 29, Day 85, Day 169, and Day 197/EOS as applicable

• Area Under the Plasma Concentration-Time Curve (AUC) Following Administration of CD388

  In both Study Periods 1 and 2 on Day 1 (pre-dose), Day 8, Day 29, Day 85, Day 169, and Day 197/EOS as applicable

Study Arms (1)

CD388

EXPERIMENTAL

Each participant will receive a single 450 mg dose of CD388 by subcutaneous (SQ) injection followed 1 year later by a repeat single 450 mg dose of CD388 administered by SQ injection.

Combination Product: CD388 Injection

Interventions

CD388 Injection COMBINATION_PRODUCT

CD388 liquid for injection

CD388

Eligibility Criteria

• Age: 18 Years - 66 Years
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Be willing and able to provide written informed consent and comply with scheduled visits, laboratory tests, and other study procedures.
• Be a male or female adult aged 18 to 66 years of age who previously completed participation in Study CD388.SQ.2.05, having received a SQ CD388 dose of either 150 mg, 300 mg or 450 mg. (Note: Participants in this study may have received seasonal influenza vaccine prior to enrollment in this study and may receive influenza vaccine during this study, with certain exceptions as described in the protocol.)
• Be in stable health at the time of screening and enrollment (in the Investigator's clinical judgment). Participants may not have a history of underlying hematologic, oncologic, renal, autoimmune, cardiac, or pulmonary conditions; or be considered at risk of developing complications from influenza infection per the United States Centers for Disease Control and Prevention (CDC) guidelines (chronic obstructive pulmonary disease \[COPD\], asthma, current immune-compromised cancer \[except non-melanomatous skin cancer\], or diabetes). Study participants will be included based on medical history and vital signs obtained during the screening process.
• Have a body mass index (BMI; calculated as weight in kilograms \[kg\] divided by height in meters \[m\] squared)) of ≥18 kg/m\^2.
• 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 enrollment and agree to remain on a highly effective method from Day 1 until 40 weeks after each study intervention administration, the end of relevant systemic exposure. Note: A female 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 females 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 from Day 1 until 40 weeks after each administration of CD388.
• Must be able to read, understand, and complete protocol questionnaires using the Sponsor-designated diary mode (eDiary or paper) and language, and be willing and able to adhere to the prohibitions and restrictions specified in this protocol. If eDiary is designated, the participant must be able to use a smartphone/tablet/computer. If an appropriate language version is not available in either eDiary or paper, the participant must not be enrolled. The diary mode and approved languages will be designated by the Sponsor prior to study start.
• Must be willing to provide verifiable identification, has means to be contacted, and is able to contact the Investigator/study site and communicate reliably during participation in this study.

You may not qualify if:

• Have a 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.
• Have an acute illness (including acute respiratory illnesses) or body temperature ≥38.0 degrees Celsius (ºC) (≥100.4 degrees Fahrenheit \[ºF\]) within 7 days prior to each administration of CD388. (Note: Enrollment and/or receipt of study intervention at a later date, subsequent to resolution of the illness \[within the screening period\], is permitted.)
• Have a serious and/or clinically unstable condition, including but not limited to, a psychiatric condition including recent (within the past year) or active suicidal ideation/behavior, Alzheimer's disease, or any other condition which in the opinion of the Investigator might lead to hospitalization or death within this study period and for which enrollment would not be in the participant's best interest, or could prevent, confound, or limit the protocol-specified assessments.
• Have any history of alcohol or substance abuse which in the opinion of the Investigator might interfere with conduct of this study as planned.
• Had major surgery (e.g., cardiac, pulmonary, neurologic, or abdominal operations) within 4 weeks prior to screening, or will not have fully recovered from such prior surgery; or has major surgery planned during the time the participant is expected to participate in this study.
• Had 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 dysrhythmia.
• Have any finding (at the time of screening) that may significantly increase the risk of participation in this study, affect the ability to participate in this study, or impair interpretation of the study data.
• Have current or planned participation in another clinical study where study intervention is being administered while participating in this 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 this present study (e.g., clinical laboratory tests).
• Have received any experimental drug, vaccine, or biologic agent within the past 90 days or 5 half-lives (whichever is longer) prior to study intervention administration.
• Have a contraindication to SQ injections and venipunctures (e.g., bleeding disorders).
• Have donated ≥450 mL of blood product (1 unit) for any reason within 30 days of screening or have plans to donate blood product during the study.
• Are currently pregnant or breastfeeding, intends to become pregnant or breastfeed, or has a positive pregnancy test during the screening period.
• Has direct involvement in the proposed study or other studies under the direction of the Investigator, sub-investigators, or study site personnel; is a family member of an individual with such direct involvement; or is an employee of the Sponsor.
• In the opinion of the Investigator, is unlikely to adhere to the requirements of this study.

Sponsors & Collaborators

• Cidara Therapeutics Inc.: lead

Study Sites (3)

Floridian Clinical Research

Miami Lakes, Florida, 33016, United States

Location

Spartanburg Medical Research

Spartanburg, South Carolina, 29303, United States

Location

hVIVO Serviced Limited

London, England, E1 1EQ, United Kingdom

Location

MeSH Terms

Conditions

Influenza, Human

Condition Hierarchy (Ancestors)

Respiratory Tract Infections; Infections; Orthomyxoviridae Infections; RNA Virus Infections; Virus Diseases; Respiratory Tract Diseases

Study Officials

• Nicole Davarpanah, MD, JD

  Cidara Therapeutics Inc.

  STUDY DIRECTOR

Study Design

• Study Type: interventional
• Phase: phase 2
• Allocation: NA
• Masking: NONE
• Purpose: PREVENTION
• Intervention Model: SINGLE GROUP
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: November 6, 2025
• First Posted: November 10, 2025
• Study Start: October 29, 2025
• Primary Completion (Estimated): July 1, 2027
• Study Completion (Estimated): July 1, 2027
• Last Updated: December 26, 2025

Record last verified: 2025-12

Data Sharing

• IPD Sharing: Will not share

Locations

US (2); GB (1)