Erythropoietic Protoporphyria (EPP)Phase 2EPPNCT06971900
GATEWAY: A Phase 2a Study of PORT-77 in Adults With Erythropoietic Protoporphyria
A Phase 2 study testing PORT-77 in people with Erythropoietic Protoporphyria (EPP), run by Portal Therapeutics, Inc. at 1 site in United States.
Trial summary
A Phase 2a study of PORT-77 in adults with erythropoietic protoporphyria (EPP) Read more about this study
- Who is it for?
- Ages 18 to 80 years
- Conditions the study is for
- Erythropoietic Protoporphyria (EPP)
- What is being tested?
- PORT-77
- Type of treatment
- Pill or oral medicine
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 28 participants
- Where
- 1 siteUnited States
- Study dates
- 4 Apr 2025to 24 Nov 2025
- Phase
- Phase 2
- Are there results?
- None posted in the registry
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 80 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Major Inclusion Criteria:
- BMI ≥18.0 and ≤40.0 kg/m2 and weight ≥50 kg on Day -1.
- Nonsmoker or willing to refrain from the use of nicotine or tobacco-containing products for at least 30 days prior to the first dose of study drug based on participant self-reporting and agrees to refrain from the use of these products throughout the study.
- Known diagnosis of EPP.
- History of consistent, non-painful prodrome prior to phototoxic attacks.
- Experiences prodrome within 40 minutes of uncovered sunlight exposure.
- Willing and able to follow protocol-specified contraception guidance.
- Able to read and understand English and is willing and able to provide document informed consent to participate in the study at the time of the Remote Screening Visit and at the In-Clinic Screening Visit.
- Able to understand the study procedures as described in the ICF and is willing and able to comply with the study requirements.
Major Exclusion Criteria:
- Is mentally or legally incapacitated or has significant emotional problems identified or observed during the screening period or expected during the conduct of the study that could lead to difficulty complying with study procedures or interfere with the safe completion of the study.
- History or presence of any illness or clinically significant medical or psychiatric condition or disease that, in the opinion of the PI or designee, might confound the results of the study or pose an additional risk to the participant by their participation in the study.
- Current alcohol or drug use disorder, as defined by the DSM-V-TR.
- History of gastrointestinal condition, including surgeries, which may affect absorption after oral administration.
- History of cancer, with the exception of cutaneous non-melanoma skin cancer (basal or squamous cell carcinoma).
- Received another investigational medicine within 5 half-lives, if the half-life is known, or within 28 days, if the half-life is unknown, prior to Day 1.
- Surgical procedure planned within 28 days prior to Day 1.
- Donation of blood or significant blood loss within 60 days prior to Day 1.
- Plasma donation within 7 days prior to Day 1.
- Unable to refrain from or anticipates the use of any of the following beginning 28 days (or 5 half-lives, whichever is longer) prior to the first dose of study drug and throughout the study:
- Substrates of BCRP or MATE1/2-K
- CYP3A4 substrates that cannot be separated by at least 2 hours from PORT-77 dosing
- Moderate or strong P-gp inhibitors or inducers
- Moderate or strong CYP3A4 inhibitors or inducers
- Herbal supplements or food products containing grapefruit juice, star fruit, or Seville oranges
- Illicit substances (eg, opiates, amphetamines, cocaine, cannabinoids [including prescription medical cannabis]).
- With the following exceptions, is unable to refrain from or anticipates the use of any nonprescription medications and herbal/nutritional supplements beginning 14 days prior to the first dose of study drug and throughout the study:
- A daily multivitamin
- Single use of acetaminophen, aspirin, or ibuprofen at a dose equal to or lower than that recommended on the package
- Estimated glomerular filtration rate <60 mL/min/1.73 m2 using the CKD-EPI equation on Day -1.
- In the absence of known mild hepatic impairment, alanine aminotransferase or aspartate aminotransferase ≥3 × ULN, or total bilirubin ≥2 × ULN (unless documented Gilbert syndrome) on Day -1.
- Moderate (Class B) or severe (Class C) hepatic impairment as measured by the Child-Pugh score reported historically or calculated on Day -1.
- Female participant with a positive pregnancy test on Day -1 or who is breastfeeding.
- Positive urine drug or alcohol results on Day -1.
- Positive results for HIV, HBsAg, or HCV antibody and HCV RNA on Day -1. Note, for participants successfully treated for HCV, positive antibody test with external laboratory evidence of negative RNA test is not exclusionary.
Trial locations and contacts
1 site in 1 country.
About this study
Official title: A Phase 2a, Blinded, Randomized, Placebo-Controlled Study of PORT-77 Administered Orally to Adults With Erythropoietic Protoporphyria
A Phase 2a study of PORT-77 in adults with erythropoietic protoporphyria (EPP)
- Conditions
- Erythropoietic Protoporphyria (EPP)
- Being tested
- PORT-77, Placebo
- Keywords
- PORT-77, EPP, erythropoietic protoporphyria
- Medical subject headings
- Protoporphyria, Erythropoietic
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
PORT-77Drug
Active oral dose form
PlaceboDrug
Matching inactive oral dose form
| Study group | Role | What they receive |
|---|---|---|
| PORT-77 | Experimental | Active Receives: Drug: PORT-77 |
| Placebo | Placebo comparator | Placebo Receives: Drug: Placebo |
What is being measured
The primary outcome is the main question the study is designed to answer.
Plasma PPIX level
Change over the course of the study in plasma PPIX concentrations
Measured: 9 Days
Secondary outcomes (9)
Safety and tolerability
Evaluate safety and tolerability of PORT-77 over the course of the study
Measured: 9 Days
Area Under the Plasma Concentration-Time Curve From Time Zero to Last Quantifiable Concentration (AUC0-last)
Area under the plasma concentration-time curve from time zero to the last measurable concentration of PORT-77
Measured: Day 1 through Day 9
Area Under the Plasma Concentration-Time Curve Over the 12-Hour Dosing Interval at Steady State (AUC0-12)
Area under the plasma concentration-time curve over the 12-hour dosing interval at steady state.
Measured: Up to Day 8
Area Under the Plasma Concentration-Time Curve Over the 24-Hour Dosing Interval at Steady State (AUC0-24)
Area under the plasma concentration-time curve over the 24-hour dosing interval at steady state.
Measured: Up to Day 8
Maximum Observed Plasma Concentration (Cmax)
Maximum observed plasma concentration of PORT-77
Measured: Day 1 through Day 9
Trough Plasma Concentration (Ctrough)
Observed plasma concentration at the end of the dosing interval.
Measured: Up to Day 8
Time to Maximum Observed Plasma Concentration (Tmax)
Time after dosing at which maximum observed plasma concentration is reached.
Measured: Day 1 through Day 9
Time of Last Quantifiable Plasma Concentration (Tlast)
Time corresponding to the last measurable plasma concentration.
Measured: Day 1 through Day 9
Terminal Elimination Half-Life (t½)
Apparent first-order terminal elimination half-life.
Measured: Day 1 through Day 9
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted14 May 2025
- Study start4 Apr 2025
- Primary completion22 Nov 2025
- Study completion24 Nov 2025
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Erythropoietic Protoporphyria (EPP)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 2
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Sequential
- Masking
- Double blind
- Who is masked
- Participant, Outcomes assessor
- Enrolment
- 28 participants (actual)
Sponsor and investigators
- Lead sponsor
- Portal Therapeutics, Inc.
- Sponsor type
- Industry (pharma, biotech, devices)
- Collaborators
- Celerion
- Responsible party
- Sponsor
- Investigators
- Chief Medical Officer, Study director, Portal Therapeutics, Inc.
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06971900
- Sponsor's protocol ID
- PORT-77-201
- Acronym
- EPP
- Status last verified
- Jul 2026
- First submitted
- 3 Apr 2025
- Last updated
- 29 Jul 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- Yes
- FDA-regulated device
- No
- Individual data sharing
- Undecided
Study at a glance
From the registry record, last updated by the sponsor on 29 Jul 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Phase 2a, Blinded, Randomized, Placebo-Controlled Study of PORT-77 Administered Orally to Adults With Erythropoietic Protoporphyria
- ClinicalTrials.gov ID
- NCT06971900
- Acronym / sponsor ID
- EPP / PORT-77-201
- Conditions
- Erythropoietic Protoporphyria (EPP)
- Keywords
- PORT-77, EPP, erythropoietic protoporphyria
- Phase
- Phase 2
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 28 participants (actual)
- Lead sponsor
- Portal Therapeutics, Inc.Industry (pharma, biotech, devices)
- Collaborators
- Celerion
- Study start
- 4 Apr 2025 (actual)
- Primary completion
- 22 Nov 2025 (actual)
- Study completion
- 24 Nov 2025 (actual)
- First posted
- 14 May 2025 (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.
A Phase 2a study of PORT-77 in adults with erythropoietic protoporphyria (EPP)
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Sequential
- Masking
- Double blind (participant, outcomes assessor)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| PORT-77 | Experimental | Drug: PORT-77Active |
| Placebo | Placebo comparator | Drug: PlaceboPlacebo |
Who may qualify
- Ages
- 18 to 80 years
- Sex
- All
- Healthy volunteers
- Not 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 |
|---|---|---|
| PORT-77Active oral dose form | Drug | PORT-77 |
| PlaceboMatching inactive oral dose form | Drug | Placebo |
Primary outcome
Plasma PPIX level
Time frame: 9 Days
Change over the course of the study in plasma PPIX concentrations
9 secondary outcomes
Safety and tolerability
Time frame: 9 Days
Area Under the Plasma Concentration-Time Curve From Time Zero to Last Quantifiable Concentration (AUC0-last)
Time frame: Day 1 through Day 9
Area Under the Plasma Concentration-Time Curve Over the 12-Hour Dosing Interval at Steady State (AUC0-12)
Time frame: Up to Day 8
Area Under the Plasma Concentration-Time Curve Over the 24-Hour Dosing Interval at Steady State (AUC0-24)
Time frame: Up to Day 8
Maximum Observed Plasma Concentration (Cmax)
Time frame: Day 1 through Day 9
Trough Plasma Concentration (Ctrough)
Time frame: Up to Day 8
Time to Maximum Observed Plasma Concentration (Tmax)
Time frame: Day 1 through Day 9
Time of Last Quantifiable Plasma Concentration (Tlast)
Time frame: Day 1 through Day 9
Terminal Elimination Half-Life (t½)
Time frame: Day 1 through Day 9
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 29 Jul 2026.
- Individual participant dataSharing planned: Undecided
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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. This study is not recruiting at the moment.
Chief Medical Officer study director
Portal Therapeutics, Inc.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 2 study testing PORT-77 in people with Erythropoietic Protoporphyria (EPP), run by Portal Therapeutics, Inc. at 1 site in United States.
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: finished, as of the sponsor's last update on 29 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 1 site in United States. 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 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Plasma PPIX level (time frame: 9 Days). 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 29 Jul 2026.