Autosomal Dominant Polycystic Kidney Disease (ADPKD)Phase 1NCT06714006
Phase 1 Study to Evaluate the Safety and Tolerability of Intravenously Administered PYC-003
A Phase 1 study testing PYC-003 in people with Autosomal Dominant Polycystic Kidney Disease (ADPKD), run by PYC Therapeutics at 12 sites in 3 countries.
Trial summary
This is a Phase 1, First-in-Human study to evaluate the safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PD) and immunogenicity of PYC-003 in healthy adult participants and adult participants with confirmed PKD1 mutation-associated Autosomal Dominant Polycystic Kidney Disease (ADPKD) There are 4 parts in… Read more about this study
- Who is it for?
- Ages 18 to 65 yearsHealthy volunteers can take part
- Conditions the study is for
- Autosomal Dominant Polycystic Kidney Disease (ADPKD)
- What is being tested?
- PYC-003
- Type of treatment
- Injection or infusion
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 166 participants
- Where
- 12 sitesin 3 countries
- Study dates
- 7 Apr 2025to Nov 2028
- Phase
- Phase 1
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 65 years
- All sexes
- Healthy volunteers accepted
- Adult, Older adult
Part A (SAD - Healthy Volunteers) Key Inclusion Criteria
- Adult aged 18 to 60 years (inclusive)
- At the discretion of the PI or designee, in good general health, with no significant medical history, and have no clinically significant abnormalities on physical examination at Screening
- BMI ≥ 18.0 and ≤ 32.0 kg/m2 and weight ≥ 50 kg.
- Non-smoker and must not have used any tobacco or nicotine products within 2 months prior to Screening.
- Clinical laboratory values within normal range or deemed not clinically significant by the PI
- eGFR ≥ 80 mL/min/1.73 m2 via the Chronic Kidney Disease Epidemiology Collaboration (CKD EPI) 2021 calculation
- Woman of childbearing potential (WOBCP) must agree to use an acceptable, highly effective, double barrier method of contraception from the start of Screening until study completion.
- Males must be surgically sterile (vasectomized for at least 6 months prior to first IP administration) or, if engaged in sexual relations with a WOCBP, must agree to use an acceptable, highly effective, double barrier method of contraception from the start of Screening until study completion.
- Females must agree not to donate ova from the first administration of IP until 30 days following study completion.
- Males must agree not donate sperm from the first administration of IP until 90 days following study completion.
- Able and willing to attend the necessary visits to the study site.
- Able and willing to adhere to caffeine, alcohol, and nicotine-containing product restrictions
- Able and willing to provide written informed consent after the nature of the study has been explained and prior to the commencement of any study procedures.
Part A (SAD - Healthy Volunteers) Key Exclusion Criteria
- Females who are pregnant, breastfeeding, or plan to become pregnant during the course of the study.
- Underlying physical or psychological medical condition that, in the opinion of the PI or designee, would make the participant unlikely to comply with the protocol or complete the study per protocol.
- Has only 1 kidney or has received a kidney transplant.
- Blood donation or had significant blood loss (> 500 mL) within 30 days prior to the first administration of IP.
- Plasma donation within 7 days prior to the first administration of IP.
- Fever (body temperature > 38°C) or symptomatic viral or bacterial infection within 2 weeks prior to first administration of IP.
- Infections requiring parenteral antibiotics within 6 months prior to Screening.
- Positive test for hepatitis C antibody (HCV), hepatitis B surface antigen (HBsAg), HIV antibody.
- History of life-threatening infection (e.g., meningitis).
- Vaccination with a live vaccine within 4 weeks prior to the first administration of IP.
- Poor venous access.
- History of severe allergic or anaphylactic reactions, or sensitivity to the IP or its constituents.
- History of malignancy, except for non-melanoma skin cancer excised more than 1 year prior to Screening and cervical intraepithelial neoplasia that has been successfully cured more than 2 years prior to Screening.
- Abnormal electrocardiogram (ECG) findings at Screening, Day -3 to Day -1, or predose that are considered by the PI or designee to be clinically significant.
- History or presence of a condition associated with significant immunosuppression.
- Exposure to any drugs that cause significant immunosuppression (including experimental therapies as part of a clinical study) within 4 months or 5 half-lives (whichever is longer), prior to Screening.
- ALP, AST, and ALT > 1.5 × ULN at Screening or Day -3 to Day -1.
- History of borderline to low blood magnesium and potassium levels and/or Screening or Day -3 to Day -1 blood magnesium level < 0.7 mmol/L and potassium levels < 3.5 mmol/L.
- Active infection of the urinary tract (ie, kidney, bladder).
- Positive toxicology screening panel (urine test including qualitative identification of amphetamines, barbiturates, benzodiazepines, cocaine, methamphetamine, methadone, opiates, phencyclidine, tetrahydrocannabinol [THC], tricyclic antidepressants), or alcohol breath test.
- History of substance abuse or dependency or history of recreational IV drug use over the last 5 years (by self-declaration).
- Regular alcohol consumption defined as > 14 standard drinks per week for females and > 21 standard drinks for males (where 1 standard drink = 375 mL of mid-strength beer [3.5% alcohol/volume], 100 mL wine [13.5% alcohol/volume] or 30 mL of spirits [40% alcohol/volume]) or > 4 standard drinks on any single day.
- Unwilling to abstain from alcohol for 48 hours prior to admission to the study site and for 48 hours prior to any follow-up visits.
- Use of any investigational medical device or investigational drug within 30 days or 5 half-lives of the investigational drug (whichever is longer) prior to the first administration of IP.
- Use of (or anticipated use of) the following:
- Any prescription drugs (other than hormonal contraception; oral contraceptive pills, long-acting implantable hormones, injectable hormones, a vaginal ring, or an intrauterine device [IUD]) within 14 days prior to the first administration of IP and during the course of the study without prior approval of the PI and MM.
- Any over-the-counter medication, herbal remedies, supplements or vitamins within 7 days prior to the first administration of IP and during the course of the study without prior approval of the PI and MM. Note: Paracetamol (i.e., up to 2000 mg per day) may be used for minor ailments during the study, at the discretion of the PI, without prior consultation with the MM.
- Unwilling to refrain from strenuous exercise (including weightlifting) for 48 hours prior to admission to the study site and for 48 hours prior to any follow-up visits.
- Anything that the PI considers would jeopardize the safety of the participant, prevent complete participation in the study, or compromise interpretation of study data.
Part B and Part C (ADPKD Participants) Key Inclusion Criteria
- Male or female aged 18 to 65 years (inclusive) at the time of informed consent.
- ADPKD diagnosis as confirmed by the presence of genetic mutations associated with ADPKD, including, but not limited to, the presence of PKD1 mutation. Note: Where genotyping is not included the medical history for a participant, genotyping may be completed at Pre-Screening.
- Class 1C, 1D, or 1E per Mayo Imaging Classification System for Predicting Kidney Outcomes in ADPKD (Irazabal et al. 2015) (based upon prior magnetic resonance imaging [MRI] or computed tomography [CT] scan obtained prior to Screening, or MRI obtained during Pre-Screening).
- BMI ≥ 18.0 and ≤ 35.0 kg/m2 and weight ≥ 50 kg.
- Non-smoker and must not have used any tobacco or nicotine products within 2 months prior to Screening.
- Estimated glomerular filtration rate (eGFR) ≥ 30 mL/min/1.73 m2 via the CKD EPI 2021 calculation
- Hematology and serum chemistry results at Screening that meet the following criteria:
- Platelets > 150 × 10^9/L
- Total white blood cell count > 3.0 × 10^9/L
- Absolute neutrophil count > 1.5 × 10^9/L
- Hemoglobin > 110 g/L for females and > 120 g/L for males
- Total and direct bilirubin < 1.5 × ULN, unless elevated bilirubin is associated with a known benign condition (e.g., Gilbert's syndrome)
- Alanine aminotransferase (ALT) < 1.5 × ULN
- Aspartate aminotransferase (AST) < 1.5 × ULN
- Alkaline phosphatase (ALP) < 1.5 × ULN
- Gamma-glutamyl transferase < 2 × ULN 9.WOCBP must agree to use an acceptable, highly effective, double barrier method of contraception from the start of Screening until study completion
- Males must be surgically sterile (vasectomized for at least 6 months prior to first administration of IP) or, if engaged in sexual relations with a WOCBP, must agree to use an acceptable, highly effective, double barrier method of contraception from the start of Screening until study completion
- Females must agree not to donate ova from the first administration of IP until 30 days following study completion. 12.Males must agree not donate sperm from the first administration of IP until 90 days following study completion.
- Able and willing to attend the necessary visits to the study site.
- Able and willing to adhere to alcohol and nicotine-containing product restrictions
- Able and willing to provide written informed consent after the nature of the study has been explained and prior to the commencement of any study procedures. Part B and Part C (ADPKD Participant) Key Exclusion Criteria
- Females who are pregnant, breastfeeding, or plan to become pregnant during the course of the study.
- Presence of potentially confounding genetic mutations (per genotyping by a NATA accredited or equivalent diagnostic laboratory)including, but not limited to, the presence of PKD2, HNF1B, GANAB, IFT140, and/or DNAJB 11 mutations.
- Use of (or anticipated use of) Tolvaptan and/or metformin administration within 30 days prior to the first administration of IP until study completion.
- Underlying physical or psychological medical condition that, in the opinion of the PI or designee, would make the participant unlikely to comply with the protocol or complete the study per protocol.
- Any renal or systemic pathology other than ADPKD or any other condition or prior therapy that in the opinion of the PI or designee would make the participant unsuitable for this study.
- Has only 1 kidney or has a kidney transplant.
- Blood donation or had significant blood loss (> 500 mL) within 30 days prior to the first administration of IP.
- Plasma donation within 7 days prior to the first administration of IP.
- Has received (or is anticipated to receive) cell therapy, gene therapy, or RNA therapy for any renal condition.
- Fever (body temperature > 38°C) or symptomatic viral or bacterial infection within 2 weeks prior to first administration of IP.
- Infections requiring parenteral antibiotics within 6 months prior to Screening.
- Positive test for hepatitis C antibody (HCV), hepatitis B surface antigen (HBsAg), HIV antibody.
- History of life-threatening infection (e.g., meningitis).
- Vaccination with a live vaccine within 4 weeks prior to the first administration of IP.
- Poor venous access.
- History of severe allergic or anaphylactic reactions, or sensitivity to the IP or its constituents.
- History of malignancy, except for non-melanoma skin cancer excised more than 1 year prior to Screening and cervical intraepithelial neoplasia that has been successfully cured more than 2 years prior to Screening.
- Abnormal ECG findings at Screening, Day -3 to Day -1, or predose that are considered by the PI or designee to be clinically significant.
- Abnormal vital signs findings at Screening that are considered by the PI or designee to be clinically significant. Note: A hypertensive participant is eligible if on a stable antihypertensive regimen for ≥ 28 days prior to first administration of IP and the blood pressure adequately controlled (per PI discretion) prior to first administration of IP.
- History or presence of a condition associated with significant immunosuppression.
- Exposure to any drugs that cause significant immunosuppression (including experimental therapies as part of a clinical study) within 4 months or 5 half-lives (whichever is longer), prior to Screening.
- History of borderline to low blood magnesium and potassium levels and/or Screening or Day -3 to Day -1 blood magnesium level < 0.7 mmol/L and potassium levels < 3.5 mmol/L.
- Urine protein: creatinine ratio (UPCR) of > 50 mg/mmol.
- Hematuria (urine protein: creatinine ratio > 30 mg/mmoL, or hematuria > ++ on dipstick, or > 100 cells per high-power field on microscopy) and/or urinary abnormalities at Screening deemed by the PI or designee to be of moderate or higher severity.
- Renal complications (eg, cyst rupture or cyst infections) within 6 weeks prior to first administration of IP.
- Active infection of the urinary tract (ie, kidney, bladder).
- Positive toxicology screening panel (urine test including qualitative identification of amphetamines, barbiturates, benzodiazepines, cocaine, methamphetamine, methadone, opiates, phencyclidine, tetrahydrocannabinol [THC], tricyclic antidepressants), or alcohol breath test.
- History of substance abuse or dependency or history of recreational IV drug use over the last 5 years (by self-declaration).
- Regular alcohol consumption defined as > 14 standard drinks per week for females and > 21 standard drinks for males (where 1 standard drink = 375 mL of mid-strength beer [3.5% alcohol/volume], 100 mL wine [13.5% alcohol/volume] or 30 mL of spirits [40% alcohol/volume]) or > 4 standard drinks on any single day.
- Unwilling to abstain from alcohol for 48 hours prior to admission to the study site and for 48 hours prior to any follow-up visits.
- Use of any investigational medical device or investigational drug within 30 days or 5 half-lives of the investigational drug (whichever is longer) prior to the first administration of IP.
- Unwilling to refrain from strenuous exercise (including weightlifting) for 48 hours prior to admission to the study site and for 48 hours prior to any follow-up visits.
- Anything that the PI considers would jeopardize the safety of the participant, prevent complete participation in the study, or compromise interpretation of study data. Part D will be an extension study for participants that complete Part C.
Trial locations and contacts
12 sites in 3 countries. Contact the study team or a site near you to ask about taking part.
12 sites in 3 countries
Australia10 sites, 10 recruiting
- Recruiting
Concord Repatriation General Hospital
Concord, New South Wales, 2139
Helen Clayton, + 61 2 9767 6576, SLHD-ConcordRenalResearch@health.nsw.gov.au
Shaundeep Sen
- Recruiting
St Vincent's Hospital Melbourne
Fitzroy, Victoria, 3056
Stephanie Thatcher, +61 427 652 661, Nephrology.Research@svha.org.au
Veena Roberts
- Recruiting
Linear Clinical Research
Joondalup, Western Australia, 6027
Brayden Ceravolo, 1300 546 327 / 08 6382 5110, enquiries@linear.org.au; bceravolo@linear.org.au
Lara Hatchuel
- Recruiting
Liverpool Hospital, Clinic G-Reception 133, Level 1, Clinical Building, Burnside Drive
Liverpool, New South Wales, 2170
Belinda Yip, +61 2 8738 7103, belinda.yip@health.nsw.gov.au
Angela Makris
- Recruiting
Scientia Clinical Research
Randwick, New South Wales, 2031
Kenneth Yong, Dr, +61 2 9382 5800, contactus@scientiaclinicalresearch.com.au
Kenneth Yong
- Recruiting
Sunshine Hospital, Western Centre for Health Research and Education, Level 3, 176-190 Furlong Road
Saint Albans, Victoria, 3021
Shannon Kokoszka, +61 3 9970 4200, shannon.kokoszka@wh.org.au
Eugenia Pedagogos
- Recruiting
Mater Hospital Brisbane
South Brisbane, Queensland, 4101
Kate O'Neill, +61 7 3163 6694, kate.oneill@mater.org.au
Michael Burke
- Recruiting
South Coast Renal, Brockway House, Level 1, Suite 8, 82-86 Queen Street,
Southport, Gold Coast, 4125
Judy Coote, +61 7 5591 2611, judy.coote@brockway.com.au
Jagadeesh Kurtkoti
- Recruiting
Sydney Adventist Hospital
Wahroonga, New South Wales, 2076
Caitlin Cirera, +61 2 9480 6283, caitleen.cirera@sah.org.au
Muhgeot Wong
- Recruiting
Westmead Hospital, Clinical Research Unit, Level 6, B Wing/Building, Hawkesbury Road
Westmead, New South Wales, 2145
Penny Murie, +61 2 8890 6848, penelope.murie@health.nsw.gov.au
Gopala Rangan
Hong Kong1 site, 1 recruiting
- Recruiting
Prince of Wales Hospital
Shatin, New Territories
Cheuk Chun Szeto, Prof, +852 35052984, ccszeto@cuhk.edu.hk
Cheuk Chun Szeto
New Zealand1 site, 1 recruiting
- Recruiting
Pacific Clinical Research Network Auckland
Takapuna, Auckland, 0622
Paul Hamilton, Dr, +64 22 585 0357, paulhamilton@pcrn.co.nz
Paul Hamilton
About this study
Official title: A Phase 1 Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of Intravenously Administered PYC-003, a Peptide-phosphorodiamidate Morpholino Oligonucleotide Conjugate, in Healthy Adult Participants and Adult Participants With Confirmed PKD1 Mutation-associated Autosomal Dominant Polycystic Kidney Disease
This is a Phase 1, First-in-Human study to evaluate the safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PD) and immunogenicity of PYC-003 in healthy adult participants and adult participants with confirmed PKD1 mutation-associated Autosomal Dominant Polycystic Kidney Disease (ADPKD) There are 4 parts in this study, i.e. Part A, Part B, Part C and Part D.
Read the detailed description
Part A (SAD - Healthy) will be conducted as a randomized, double-blind, placebo-controlled, SAD study to assess the safety, tolerability, PK, PD, and immunogenicity of PYC-003 in healthy adult participants.
The anticipated number of participants across 5 Part A (SAD - Healthy) cohorts is approximately 40 participants.
On Day 1, each participant will receive the investigational product (IP; ie, PYC-003 or placebo), as a single intravenous (IV) infusion.
Part B (SAD - ADPKD) will be conducted as an open-label single ascending dose (SAD) study to assess the safety, tolerability, PK, PD, and immunogenicity of PYC-003 in adult participants with confirmed PKD1 mutation-associated ADPKD. The anticipated number of participants across 5 Part B (SAD - ADPKD) cohorts is approximately 30 participants. On Day 1, each participant will receive PYC-003 as a single IV infusion.
Part C (MAD-ADPKD) will be conducted as an open label multiple ascending dose (MAD) study to assess the safety, tolerability, PK, PD, and immunogenicity of PYC-003 in adult participants with confirmed PKD1 mutation-associated ADPKD. The anticipated number of participants across 4 Part C (MAD - ADPKD) cohorts is approximately 48-96 participants. Each participant will receive PYC-003 as an IV infusion either once every 6 weeks for 13 weeks or once every 8 weeks for 17 weeks.
Part D will be an extension study for participants that complete Part C where participants will continue receiving doses for up to 96 weeks.
- Being tested
- PYC-003
- Keywords
- PKD1, Autosomal Dominant Polycystic Kidney Disease, ADPKD
- Medical subject headings
- Polycystic Kidney, Autosomal Dominant
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
PYC-003Drug
A peptide-phosphorodiamidate morpholino oligonucleotide conjugate administered as a single intravenous infusion
| Study group | Role | What they receive |
|---|---|---|
| Part A (SAD - Healthy) | Placebo comparator | Part A will be conducted as a randomized, double-blend, placebo-controlled, Single Ascending Dose Study in healthy adult participants. On Day 1, each participant will receive the investigational product (IP; i.e., PYC-003 or placebo), as a single intravenous (IV) infusion. All Part A (SAD - Healthy) cohorts will first dose 2 sentinel participants in a blinded manner on Day 1. Receives: Drug: PYC-003 |
| Part B (SAD - ADPKD) | Experimental | Part B will be conducted as an open-label Single Ascending Dose study in adult participants with confirmed PKD1 mutation-associated ADPKD. On Day 1, each participant will receive PYC-003 as a single IV infusion. Receives: Drug: PYC-003 |
| Part C (MAD - ADPKD) | Experimental | Part C (MAD - ADPKD) will be conducted as an open-label MAD study in adult participants with confirmed PKD1 mutation-associated ADPKD. Each participant will receive PYC-003 as an IV infusion either once every 6 weeks for 13 weeks (i.e., dosing on Day 1, Day 43, and Day 85) or once every 8 weeks for 17 weeks (i.e., dosing on Day 1, Day 57, and Day 113). Receives: Drug: PYC-003 |
| Part D - Open Label Extension | Experimental | Part D will be an extension study for participants that complete Part C. Participants will receive doses either every 6 or 8 weeks for 96 weeks . Receives: Drug: PYC-003 |
What is being measured
The primary outcome is the main question the study is designed to answer.
[Part A, B, C and D] Number of participants experiencing treatment emergent adverse events (AE) as assessed by CTCAE V5.0
The incidence, severity, and relatedness of treatment emergent adverse events and treatment-emergent Serious Adverse Events will be recorded
An AE is any event, side-effect, or other untoward medical occurrence that occurs in conjunction with the use of a medicinal product in humans, whether or not considered to have a causal relationship to this treatment. An AE can, therefore, be any unfavourable and unintended sign (that could include a clinically significant abnormal laboratory finding), symptom, or disease temporally associated with the use of a medicinal product, whether or not considered related to the medicinal product.
Measured: Up to 98 weeks
[Part A, B, C and D] Changes from baseline in vital signs (body temperature)
Measured: Up to 98 weeks
[Part A, B, C and D] Changes from baseline in vital signs (systolic and diastolic blood pressure)
Measured: Up to 98 weeks
[Part A, B, C and D] Changes from baseline in vital signs (pulse rate)
Measured: Up to 98 weeks
[Part A, B, C and D] Changes from baseline in vital signs (respiratory rate)
Measured: Up to 98 weeks
[Part A, B, C and D] Changes from baseline in 12-lead ECG (QT Interval)
Measured: Up to 98 weeks
[Part A, B, C and D] Changes from baseline in 12-lead ECG (QRS Duration)
Measured: Up to 98 weeks
[Part A, B, C and D] Changes from baseline in 12-lead ECG (QTcF Interval)
Measured: Up to 98 weeks
[Part A, B, C and D] Changes from baseline in 12-lead ECG (PR Interval)
Measured: Up to 98 weeks
[Part A, B, C and D] Changes from baseline in 12-lead ECG (Heart Rate)
Measured: Up to 98 weeks
[Part A, B, C and D] Changes from baseline in physical examination findings
Complete physical examinations include general appearance, head, ears, eyes, nose, throat, dentition, thyroid, chest (heart, lungs), abdomen, skin, neurological, extremities, back, neck, musculoskeletal, and lymph nodes.
Abbreviated physical examinations will be symptom directed.
Measured: Up to 98 weeks
[Part A, B, C and D] Changes from baseline in hepatic clinical chemistry parameters (ALT, AST, ALP and GGT)
ALT (Alanine Transaminase), AST (Aspartate Transaminase) ALP (Alkaline Phosphatase) and GGT (Gamma-glutamyl transferase) will be tested
Measured: Up to 98 weeks
[Part A, B, C and D] Changes from baseline in standard renal clinical chemistry parameters (eGFR)
estimated Glomerular filtration rate (eGFR) will be calculated via the CKD EPI 2021 calculation
Measured: Up to 98 weeks
[Part A, B, C and D] Changes from baseline in serum potassium, serum magnesium, and serum sodium
Measured: Up to 98 weeks
[Part A, B, C and D] Changes from baseline in serum cystatin C
Measured: Up to 98 weeks
[Part A, B, C and D] Changes from baseline in serum and urine creatinine
Measured: Up to 98 weeks
[Part A, B, C and D] Changes from baseline in serum and urine osmolality
Measured: Up to 98 weeks
[Part A, B, C and D] Changes from baseline in urine magnesium and urine potassium
Measured: Up to 98 weeks
Secondary outcomes (10)
[Part A, B, C and D] Peak plasma concentration (Cmax) of PYC003
Measured: Up to 98 weeks
[Part A, B, C and D] Time to maximum observed plasma drug concentration (Tmax) of PYC003
Measured: Up to 98 weeks
[Part A, B and C] Area under the plasma concentration-time curve, from time zero to 24 hours post dose of PYC-003 (AUC0-24)
Measured: Up to 36 weeks
[Part A, B and C] Area under the plasma concentration-time curve, from time zero to the last time point with measurable analyte concentration after PYC-003 dose (AUC0-last)
Measured: Up to 36 weeks
[Part A, B and C] Area under the plasma concentration-time curve, from time zero extrapolated to infinity (AUC0-inf)
Measured: Up to 36 weeks
[Part A, B and C] The percentage of the AUC that was extrapolated beyond the last observed data point (AUC%extrap)
Measured: Up to 36 weeks
[Part A, B and C] Apparent half life of PYC-003 (T1/2)
Measured: Up to 36 weeks
[Part A, B and C] Apparent elimination constant (Kel) of PYC-003
Measured: Up to 36 weeks
[Part A, B and C] Apparent clearance (CL) of PYC-003
Measured: Up to 36 weeks
[Part A, B and C] Apparent volume of distribution (Vz) of PYC-003
Measured: Up to 36 weeks
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted3 Dec 2024
- Study start7 Apr 2025
- Primary completionNov 2028 (estimated)
- Study completionNov 2028 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Autosomal Dominant Polycystic Kidney Disease (ADPKD)Studies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 1
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Model description
- The study comprises of 4 parts: Part A (SAD - Healthy) will be conducted as a randomized, double-blind, placebo-controlled, SAD study -and will enroll healthy adult participants. On Day 1, each participant will receive either PYC-003 or placebo, as a single intravenous (IV) infusion. Part B (SAD - ADPKD) will be conducted as an open-label SAD study in adult participants with confirmed PKD1 mutation-associated ADPKD. On Day 1, each participant will receive PYC-003 as a single IV infusion. Part C (MAD-ADPKD) will be conducted as an open label multiple ascending dose (MAD) study in adult participants with confirmed PKD1 mutation-associated ADPKD. Each participant will receive 3 doses of PYC-003 either 6 weeks or 8 weeks apart. Part D will be an extension study for participants that complete Part C where participants will continue receiving doses either 6 or 8 weeks apart for up to 96 weeks.
- Masking
- Triple blind
- Who is masked
- Participant, Investigator, Outcomes assessor
- Enrolment
- 166 participants (estimated)
Sponsor and investigators
- Lead sponsor
- PYC Therapeutics
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06714006
- Sponsor's protocol ID
- PYC-003-CL-001
- Status last verified
- Jul 2026
- First submitted
- 24 Nov 2024
- Last updated
- 27 Jul 2026
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 27 Jul 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Phase 1 Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of Intravenously Administered PYC-003, a Peptide-phosphorodiamidate Morpholino Oligonucleotide Conjugate, in Healthy Adult Participants and Adult Participants With Confirmed PKD1 Mutation-associated Autosomal Dominant Polycystic Kidney Disease
- ClinicalTrials.gov ID
- NCT06714006
- Acronym / sponsor ID
- PYC-003-CL-001
- Keywords
- PKD1, Autosomal Dominant Polycystic Kidney Disease, ADPKD
- Phase
- Phase 1
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 166 participants (estimated)
- Lead sponsor
- PYC TherapeuticsIndustry (pharma, biotech, devices)
- Study start
- 7 Apr 2025 (actual)
- Primary completion
- Nov 2028 (estimated)
- Study completion
- Nov 2028 (estimated)
- First posted
- 3 Dec 2024 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This is a Phase 1, First-in-Human study to evaluate the safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PD) and immunogenicity of PYC-003 in healthy adult participants and adult participants with confirmed PKD1 mutation-associated Autosomal Dominant Polycystic Kidney Disease (ADPKD) There are 4 parts in this study, i.e. Part A, Part B, Part C and Part D.
Detailed description
Part A (SAD - Healthy) will be conducted as a randomized, double-blind, placebo-controlled, SAD study to assess the safety, tolerability, PK, PD, and immunogenicity of PYC-003 in healthy adult participants.
The anticipated number of participants across 5 Part A (SAD - Healthy) cohorts is approximately 40 participants.
On Day 1, each participant will receive the investigational product (IP; ie, PYC-003 or placebo), as a single intravenous (IV) infusion.
Part B (SAD - ADPKD) will be conducted as an open-label single ascending dose (SAD) study to assess the safety, tolerability, PK, PD, and immunogenicity of PYC-003 in adult participants with confirmed PKD1 mutation-associated ADPKD. The anticipated number of participants across 5 Part B (SAD - ADPKD) cohorts is approximately 30 participants. On Day 1, each participant will receive PYC-003 as a single IV infusion.
Part C (MAD-ADPKD) will be conducted as an open label multiple ascending dose (MAD) study to assess the safety, tolerability, PK, PD, and immunogenicity of PYC-003 in adult participants with confirmed PKD1 mutation-associated ADPKD. The anticipated number of participants across 4 Part C (MAD - ADPKD) cohorts is approximately 48-96 participants. Each participant will receive PYC-003 as an IV infusion either once every 6 weeks for 13 weeks or once every 8 weeks for 17 weeks.
Part D will be an extension study for participants that complete Part C where participants will continue receiving doses for up to 96 weeks.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Triple blind (participant, investigator, outcomes assessor)
- Number of arms
- 4
- Model description
- The study comprises of 4 parts: Part A (SAD - Healthy) will be conducted as a randomized, double-blind, placebo-controlled, SAD study -and will enroll healthy adult participants. On Day 1, each participant will receive either PYC-003 or placebo, as a single intravenous (IV) infusion. Part B (SAD - ADPKD) will be conducted as an open-label SAD study in adult participants with confirmed PKD1 mutation-associated ADPKD. On Day 1, each participant will receive PYC-003 as a single IV infusion. Part C (MAD-ADPKD) will be conducted as an open label multiple ascending dose (MAD) study in adult participants with confirmed PKD1 mutation-associated ADPKD. Each participant will receive 3 doses of PYC-003 either 6 weeks or 8 weeks apart. Part D will be an extension study for participants that complete Part C where participants will continue receiving doses either 6 or 8 weeks apart for up to 96 weeks.
| Arm | Type | Receives |
|---|---|---|
| Part A (SAD - Healthy) | Placebo comparator | Drug: PYC-003Part A will be conducted as a randomized, double-blend, placebo-controlled, Single Ascending Dose Study in healthy adult participants. On Day 1, each participant will receive the investigational product (IP; i.e., PYC-003 or placebo), as a single intravenous (IV) infusion. All Part A (SAD - Healthy) cohorts will first dose 2 sentinel participants in a blinded manner on Day 1. |
| Part B (SAD - ADPKD) | Experimental | Drug: PYC-003Part B will be conducted as an open-label Single Ascending Dose study in adult participants with confirmed PKD1 mutation-associated ADPKD. On Day 1, each participant will receive PYC-003 as a single IV infusion. |
| Part C (MAD - ADPKD) | Experimental | Drug: PYC-003Part C (MAD - ADPKD) will be conducted as an open-label MAD study in adult participants with confirmed PKD1 mutation-associated ADPKD. Each participant will receive PYC-003 as an IV infusion either once every 6 weeks for 13 weeks (i.e., dosing on Day 1, Day 43, and Day 85) or once every 8 weeks for 17 weeks (i.e., dosing on Day 1, Day 57, and Day 113). |
| Part D - Open Label Extension | Experimental | Drug: PYC-003Part D will be an extension study for participants that complete Part C. Participants will receive doses either every 6 or 8 weeks for 96 weeks . |
Who may qualify
- Ages
- 18 to 65 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| PYC-003A peptide-phosphorodiamidate morpholino oligonucleotide conjugate administered as a single intravenous infusion | Drug | Part A (SAD - Healthy), Part B (SAD - ADPKD), Part C (MAD - ADPKD), Part D - Open Label Extension |
Primary outcome
[Part A, B, C and D] Number of participants experiencing treatment emergent adverse events (AE) as assessed by CTCAE V5.0
Time frame: Up to 98 weeks
The incidence, severity, and relatedness of treatment emergent adverse events and treatment-emergent Serious Adverse Events will be recorded An AE is any event, side-effect, or other untoward medical occurrence that occurs in conjunction with the use of a medicinal product in humans, whether or not considered to have a causal relationship to this treatment. An AE can, therefore, be any unfavourable and unintended sign (that could include a clinically significant abnormal laboratory finding), symptom, or disease temporally associated with the use of a medicinal product, whether or not considered related to the medicinal product.
[Part A, B, C and D] Changes from baseline in vital signs (body temperature)
Time frame: Up to 98 weeks
[Part A, B, C and D] Changes from baseline in vital signs (systolic and diastolic blood pressure)
Time frame: Up to 98 weeks
[Part A, B, C and D] Changes from baseline in vital signs (pulse rate)
Time frame: Up to 98 weeks
[Part A, B, C and D] Changes from baseline in vital signs (respiratory rate)
Time frame: Up to 98 weeks
[Part A, B, C and D] Changes from baseline in 12-lead ECG (QT Interval)
Time frame: Up to 98 weeks
[Part A, B, C and D] Changes from baseline in 12-lead ECG (QRS Duration)
Time frame: Up to 98 weeks
[Part A, B, C and D] Changes from baseline in 12-lead ECG (QTcF Interval)
Time frame: Up to 98 weeks
[Part A, B, C and D] Changes from baseline in 12-lead ECG (PR Interval)
Time frame: Up to 98 weeks
[Part A, B, C and D] Changes from baseline in 12-lead ECG (Heart Rate)
Time frame: Up to 98 weeks
[Part A, B, C and D] Changes from baseline in physical examination findings
Time frame: Up to 98 weeks
Complete physical examinations include general appearance, head, ears, eyes, nose, throat, dentition, thyroid, chest (heart, lungs), abdomen, skin, neurological, extremities, back, neck, musculoskeletal, and lymph nodes. Abbreviated physical examinations will be symptom directed.
[Part A, B, C and D] Changes from baseline in hepatic clinical chemistry parameters (ALT, AST, ALP and GGT)
Time frame: Up to 98 weeks
ALT (Alanine Transaminase), AST (Aspartate Transaminase) ALP (Alkaline Phosphatase) and GGT (Gamma-glutamyl transferase) will be tested
[Part A, B, C and D] Changes from baseline in standard renal clinical chemistry parameters (eGFR)
Time frame: Up to 98 weeks
estimated Glomerular filtration rate (eGFR) will be calculated via the CKD EPI 2021 calculation
[Part A, B, C and D] Changes from baseline in serum potassium, serum magnesium, and serum sodium
Time frame: Up to 98 weeks
[Part A, B, C and D] Changes from baseline in serum cystatin C
Time frame: Up to 98 weeks
[Part A, B, C and D] Changes from baseline in serum and urine creatinine
Time frame: Up to 98 weeks
[Part A, B, C and D] Changes from baseline in serum and urine osmolality
Time frame: Up to 98 weeks
[Part A, B, C and D] Changes from baseline in urine magnesium and urine potassium
Time frame: Up to 98 weeks
10 secondary outcomes
[Part A, B, C and D] Peak plasma concentration (Cmax) of PYC003
Time frame: Up to 98 weeks
[Part A, B, C and D] Time to maximum observed plasma drug concentration (Tmax) of PYC003
Time frame: Up to 98 weeks
[Part A, B and C] Area under the plasma concentration-time curve, from time zero to 24 hours post dose of PYC-003 (AUC0-24)
Time frame: Up to 36 weeks
[Part A, B and C] Area under the plasma concentration-time curve, from time zero to the last time point with measurable analyte concentration after PYC-003 dose (AUC0-last)
Time frame: Up to 36 weeks
[Part A, B and C] Area under the plasma concentration-time curve, from time zero extrapolated to infinity (AUC0-inf)
Time frame: Up to 36 weeks
[Part A, B and C] The percentage of the AUC that was extrapolated beyond the last observed data point (AUC%extrap)
Time frame: Up to 36 weeks
[Part A, B and C] Apparent half life of PYC-003 (T1/2)
Time frame: Up to 36 weeks
[Part A, B and C] Apparent elimination constant (Kel) of PYC-003
Time frame: Up to 36 weeks
[Part A, B and C] Apparent clearance (CL) of PYC-003
Time frame: Up to 36 weeks
[Part A, B and C] Apparent volume of distribution (Vz) of PYC-003
Time frame: Up to 36 weeks
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 27 Jul 2026.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
12 sites in 3 countries: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 1 study testing PYC-003 in people with Autosomal Dominant Polycystic Kidney Disease (ADPKD), run by PYC Therapeutics at 12 sites in 3 countries.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: looking for participants now, as of the sponsor's last update on 27 Jul 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 12 sites in Australia, Hong Kong, New Zealand. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this phase mean?
Phase 1 studies test a treatment in a small group of people for the first time or in a new way, mainly to check safety and find the right dose.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Paula Cunningham Chief Preclinical Research Officer (+61 8 6151 0992., pkd@pyctx.com), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
[Part A, B, C and D] Number of participants experiencing treatment emergent adverse events (AE) as assessed by CTCAE V5.0 (time frame: Up to 98 weeks). The study lists 18 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 27 Jul 2026; AzTrials last refreshed its copy on 31 Oct 2026.