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Trial details imported from ClinicalTrials.gov

For full trial details, please see the original record at https://clinicaltrials.gov/study/NCT06903611




Registration number
NCT06903611
Ethics application status
Date submitted
25/03/2025
Date registered
31/03/2025
Date last updated
18/05/2025

Titles & IDs
Public title
Phase III Study of Topical Fibrinogen-Depleted Human Platelet Lysate Compared to Placebo for Moderate to Severe Dry Eye
Scientific title
CAMOMILE-3: Phase III Randomized, Double-Masked, Safety and Efficacy Study of Topical Fibrinogen-Depleted Human Platelet Lysate Compared to Vehicle Control for the Treatment of Moderate to Severe Dry Eye
Secondary ID [1] 0 0
CAM-101-003
Universal Trial Number (UTN)
Trial acronym
CAMOMILE-3
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Dry Eye Disease 0 0
Dry Eye 0 0
Dry Eyes Chronic 0 0
Dry Eye Syndromes 0 0
Condition category
Condition code
Eye 0 0 0 0
Diseases / disorders of the eye

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Treatment: Drugs - CAM-101
Other interventions - Vehicle Control

Placebo comparator: 1-Vehicle Control Group - Vehicle Control Group - masked treatment with vehicle control for 9 weeks. Instill 1 drop in both eyes 4 times per day for 9 weeks.

Experimental: 2-Active Treatment Group - CAM-101 Active Group - masked treatment with CAM-101 for 9 weeks; Instill 1 drop in both eyes 4 times per day for 9 weeks. Open label use long term follow up: CAM-101, install 1 drop in both eyes 4 times per day for 43 weeks if the patient was on active IP during the 9 week randomized study or 52 weeks if the patient was on vehicle during the 9 week randomized study


Treatment: Drugs: CAM-101
fibrinogen depleted human platelet lysate

Other interventions: Vehicle Control
Plasmalyte-A
Intervention code [1] 0 0
Treatment: Drugs
Intervention code [2] 0 0
Other interventions
Comparator / control treatment
Control group

Outcomes
Primary outcome [1] 0 0
Corneal Fluorescein
Timepoint [1] 0 0
9 weeks
Primary outcome [2] 0 0
Eye Discomfort
Timepoint [2] 0 0
9 weeks

Eligibility
Key inclusion criteria
1. Male or female subjects who at the time of consent are 18 years of age or older, if participating at a study site located in the U.S.; or 20 years of age or older if participating at a study site located in India.
2. Having a self-reported history of dry eye disease within the past 6 months.
3. NEI Corneal Fluorescein Staining Score in at least one eye at screening and at Day 0 (pre-randomization) that is = 6= 6 (total score)as determined by the investigator.
4. Visual Analog Scale (VAS) Symptom Index-Eye Dryness/Eye Discomfort total score (pre-dose) that is = 40 points at screening and at Day 0 (pre-randomization).
5. Willingness to have both the right and left eyes treated in the study.
6. Willingness to discontinue contact lenses and all current DED treatments except artificial tears.
7. Be able to demonstrate ability to use study medication bottle; this can be documented on study bottle used during washout period.
8. Female subjects must be either: (1) of non-childbearing potential; or, (2) of childbearing potential and using an acceptable method of birth control with a negative pregnancy test :

1. Females of Non-childbearing Potential: Surgically sterilized (e.g., hysterectomy or bilateral oophorectomy) prior to screening; or, post-menopausal (i.e., no menstrual bleeding for at least 1 year prior to screening; or with a negative pregnancy test if less than 1 year post-menopausal).
2. Females of Childbearing Potential: Must agree to use a highly effective acceptable form of birth control (e.g., established hormonal birth control, or double barrier method: intrauterine device plus condom or spermicidal gel plus condom) from 21 days prior to dosing until 7 days after dosing.
9. Providing written Informed Consent consistent with privacy language as per national regulations (e.g., HIPAA authorization) with signature obtained from the subject or legally authorized representative prior to the performance of any study related procedures (including withdrawal of prohibited medication.
10. Willingness and ability to comply with schedule for follow-up visits and postoperative evaluations.

-
Minimum age
18 Years
Maximum age
No limit
Sex
Both males and females
Can healthy volunteers participate?
Yes
Key exclusion criteria
* Subjects who meet any of the following exclusion criteria for one or both eyes at screening will not be enrolled in the study. Subjects who meet any of the following exclusion criteria for one or both eyes on Day 0 will not be randomized and will be withdrawn from the study as screen failures:

1. Any abnormal lid anatomy or blinking function in either eye.
2. Using any topical ocular treatment other than the following medications:

a. Artificial Tears: Preservative-free artificial tears may be used as needed before and/or during the study. Whenever practicable, the same brand of artificial tears should be used throughout the study and its use documented in the patient diary throughout study participation.
3. Previous ocular surgery of any type (including lacrimal, corneal and trauma), except:

1. Non-refractive laser eye surgery of any type in either eye performed more than 3 months before screening is permitted.
2. Refractive surgery in either eye performed more than 6 months before screening is permitted.
3. Cataract surgery in either eye performed more than 3 months before screening is permitted
4. Any ocular anomaly that, in the investigator's opinion, interferes with the ocular surface, including:

1. Active ocular herpes simplex virus infection
2. Recurrent corneal erosion
3. Symptomatic epithelial basement membrane dystrophy
4. Mucus fishing syndrome
5. Giant papillary conjunctivitis
6. Post-radiation keratitis
7. Stevens-Johnson syndrome
8. Corneal ulcer
9. Abnormalities of the nasolacrimal drainage system
10. Chemical injury
11. Diagnosed significant anterior blepharitis and/or progressive pterygium
5. Current history of ocular infection (viral, bacterial, fungal), disease or inflammation (e.g., uveitis) not associated with dry eye, unless the disorder or disease is, in the investigator's opinion:

1. Stable for at least 3 months before the Screening Visit; and,
2. Not likely to impact or possibly interfere with the interpretation of study results.
6. Subjects with a current intraocular infection or with any other current eye or systemic condition (e.g., severe endothelial corneal dystrophy) that, in the investigator's opinion, would interfere with the dry eye evaluation or treatment, or for which the potential benefits of CAM-101 do not outweigh the risks.
7. History of ocular allergy (including seasonal conjunctivitis) or chronic conjunctivitis other than that secondary to dry eye.
8. Known hypersensitivity to the components of CAM-101 or the vehicle control (fibrinogen-depleted human platelet lysate; Plasma-Lyte A).
9. Known hypersensitivity to one of the procedural medications (e.g., proparacaine, fluorescein) unless a suitable alternative medication is available.
10. Inability to refrain from contact lens wear during the study, including the vehicle control run-in period.
11. Anticipated need for temporary or permanent punctum plugs during the study. (If punctum plugs have been in place for at least 4 weeks prior to the screening visit, the plugs are allowed to remain in place during the study. ) Patients must remain symptomatic for DED post punctal plug insertion.
12. Any ocular disease or ocular condition not stabilized within 1 month (30 days) before the screening visit.
13. Any clinically significant systemic disease or condition that is inadequately controlled (e.g., diabetes, thyroid disease, autoimmune disease) or not stabilized within 4 weeks before the screening visit.
14. Inability or unwillingness to discontinue use of autologous serum eye drops or platelet rich plasma eye drops during the 2-week run-in period and throughout the remainder of the study.
15. Female subjects who are pregnant or lactating or plan to become pregnant during the course of the study.
16. Subjects not under legal guardianship who, in the investigator's opinion, lack the mental capacity to provide written informed consent for study participation.

Study design
Purpose of the study
Treatment
Allocation to intervention
Randomised controlled trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Masking / blinding
Blinded (masking used)
Who is / are masked / blinded?
The people receiving the treatment/s
The people administering the treatment/s
The people assessing the outcomes
The people analysing the results/data
Intervention assignment
Crossover
Other design features
Phase
Phase 3
Type of endpoint/s
Statistical methods / analysis

Recruitment
Recruitment status
Not yet recruiting
Data analysis
Reason for early stopping/withdrawal
Other reasons
Date of first participant enrolment
Anticipated
30/09/2025
Actual
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
1/12/2027
Actual
Sample size
Target
400
Accrual to date
Final
Recruitment in Australia
Recruitment state(s)

Funding & Sponsors
Primary sponsor type
Commercial sector/industry
Name
Cambium Bio Limited
Address
Country

Ethics approval
Ethics application status

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 0 0
Neera Jagirdar, MD MPH
Address 0 0
Cambium Bio Limited
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for public queries
Name 0 0
VP, Medical, Clinical & Regulatory Affairs
Address 0 0
Country 0 0
Phone 0 0
6175929138
Fax 0 0
Email 0 0
[email protected]
Contact person for scientific queries

No information has been provided regarding IPD availability


What supporting documents are/will be available?

No Supporting Document Provided


Results publications and other study-related documents

No documents have been uploaded by study researchers.

Results not provided in https://clinicaltrials.gov/study/NCT06903611