A Dose Escalation Trial Evaluating Safety, Efficacy, and Pharmacokinetics of Multiple Subcutaneous Doses of TransCon CNP Administered Once Weekly in Children With Achondroplasia
Study Details
Study Description
Brief Summary
Purpose of the study:
The main purpose of this study is to determine the safety and evaluate the effect of a once weekly dose of TransCon CNP in prepubertal children with achondroplasia in China.
Study Treatments:
TransCon CNP is an investigational (new) drug, which means that it is currently being tested, and therefore is considered experimental. TransCon CNP is designed to provide a sustained exposure of active CNP by subcutaneous (under the skin) injection once weekly.
The Randomized Period of this study is a double-blinded and placebo-controlled. "Placebo-controlled" means that some participants will receive injections that don't contain any TransCon CNP (placebo injection - no active ingredient). "Double-blinded" means that neither the participant nor the study doctor will know which treatment the participant will be receiving, except in an emergency.
After completion of the Randomized Period the trial participant may be invited to take part of the Open-Label Period of this study.
"Open-label" means that all participants will receive injections that contain TransCon CNP; regardless of which treatment (TransCon CNP or placebo) was assigned during the 52 weeks (1 year) Randomized Period/blinded treatment period. It also means that both the participant and the study doctor will know which treatment, and which dose the participant receives.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Phase 2 |
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: TransCon CNP 50 mcg TransCon CNP 50 mcg CNP/kg or placebo mimicking TransCon CNP 50 mcg delivered once weekly by subcutaneous injection |
Drug: TransCon CNP
TransCon CNP drug product is a lyophilized powder in a single-use vial containing either TransCon CNP 3.9 mg CNP-38/vial or TransCon CNP 0.80 mg CNP-38/vial. Prior to use, the lyophilized powder is reconstituted with sterile water for injection and administered by subcutaneous injection via syringe and needle.
Drug: Placebo for TransCon CNP
Weekly subcutaneously injection of placebo.
|
| Experimental: TransCon CNP 100 mcg TransCon CNP 100 mcg CNP/kg or placebo mimicking TransCon CNP 100 mcg delivered once weekly by subcutaneous injection |
Drug: TransCon CNP
TransCon CNP drug product is a lyophilized powder in a single-use vial containing either TransCon CNP 3.9 mg CNP-38/vial or TransCon CNP 0.80 mg CNP-38/vial. Prior to use, the lyophilized powder is reconstituted with sterile water for injection and administered by subcutaneous injection via syringe and needle.
Drug: Placebo for TransCon CNP
Weekly subcutaneously injection of placebo.
|
| Experimental: TransCon CNP >100 mcg TransCon CNP >100 mcg CNP/kg delivered once weekly by subcutaneous injection (to be determined after completion of 100 mcg cohort) |
Drug: TransCon CNP
TransCon CNP drug product is a lyophilized powder in a single-use vial containing either TransCon CNP 3.9 mg CNP-38/vial or TransCon CNP 0.80 mg CNP-38/vial. Prior to use, the lyophilized powder is reconstituted with sterile water for injection and administered by subcutaneous injection via syringe and needle.
Drug: Placebo for TransCon CNP
Weekly subcutaneously injection of placebo.
|
Outcome Measures
Primary Outcome Measures
- Incidence of Treatment-Emergent Adverse Events (Safety and Tolerability) [52 weeks]
Safety and tolerability of once weekly TransCon CNP treatment or placebo
- Annualized height velocity (centimeters/year) at 52 weeks [52 weeks]
Annualized height velocity measured in centimeters over 52 weeks for TransCon CNP or placebo
Eligibility Criteria
Criteria
Inclusion Criteria:
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Diagnosis of achondroplasia confirmed by genetic testing
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Age criteria: between ages 2 to 10 years old (inclusive) at Screening Visit
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Tanner stage 1 breast development for females or testicular volume < 4ml for males at Screening
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Able to stand without assistance
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Parent/ legal guardian willing and able to administer subcutaneous injections of study medication
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Written, signed informed consent of the parent(s) or legal guardian(s) of the participant and written assent of the participant as required by the institutional review board/human research ethics committee/independent ethics committee (IRB/HREC/IEC)
Exclusion Criteria:
- Clinically significant findings at Screening that:
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Are expected to require surgical intervention during participation in the trial or
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Are musculoskeletal in nature, such as Salter-Harris fractures or severe hip pain or
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Otherwise are considered by the Investigator or Medical Monitor to make a participant unfit to receive investigational medicinal products or undergo trial related procedures
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Have received any dose of prescription medications intended to affect stature or body proportionality (including human growth hormone) in the 6 months prior to Screening (excluding nutritional supplements)
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Have received any investigational medicinal product or device intended to affect stature or body proportionality at any time
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History or presence of injury or disease of the growth plate(s), other than ACH, that affects growth potential of long bones
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History of any bone-related surgery that affects growth potential of long bones, such as orthopedic reconstructive surgery, including but not limited to:
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Foramen magnum decompression and laminectomy with full recovery are allowed with minimum of 6 months of bone healing
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Osteotomy to correct bowing is allowed with 12 months of bone healing
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Limb-lengthening with full recovery is allowed with a minimum of 12 months of bone healing
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History of 8 plate epiphysiodesis is allowed, but the plates must have been removed prior to Screening with minimum of 4 weeks of healing
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Have a growth disorder other than ACH that results in short stature or abnormal growth such as severe achondroplasia with developmental delay and acanthosis nigricans (SADDAN), hypochondroplasia, growth hormone deficiency, Turner syndrome, or pseudoachondroplasia
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Have a medical condition that could result in short stature or abnormal growth such as inflammatory bowel disease, celiac disease, vitamin D deficiency, untreated hypothyroidism, or poorly controlled diabetes mellitus (HbA1c ≥8.0%), or other diabetic complications. Please note the following allowances:
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Vitamin D deficiency or insufficiency treated with supplementation is allowed. Vitamin D deficiency is defined as 25(OH)D level <20ng/mL (<49.9 nmol/L), insufficiency is defined as 25(OH)D level <20-30ng/mL (49.92 - 74.86 nmol/L). Participants with Vitamin D deficiency or insufficiency must be on Vitamin D regimen before enrollment
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Participants with hypothyroidism must be clinically euthyroid for 3 months prior to enrollment and, in the opinion of the Investigator, have achieved any catch-up growth expected from thyroxine replacement
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Participants with diabetes mellitus must have been on a stable medication regimen for 3 months prior to enrollment (dose adjustments are allowed but addition or discontinuation of medications in this time period is disallowed). In addition to HbA1c <8.0%, any participant with diabetes must have adequate glycemic control in the opinion of the Investigator and Medical Monitor to be considered a good candidate for the trial
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History or presence of malignant disease, other than basal cell epithelioma/carcinoma or completely resected squamous skin cancer with no recurrence for 12 months per medical records
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History or presence of the following:
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Chronic anemia (iron deficiency anemia that is resolved or adequately treated in the Investigator's opinion is allowed)
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Significant cardiovascular disease per the judgement of the Investigator, such as congenital heart disease (uncomplicated patent ductus arteriosus and atrial or ventricular septal defect with repair are allowed), aortic insufficiency, clinically significant arrhythmias, congestive heart failure with NYHA class II and above or other conditions that impair regulation of blood pressure or heart rate
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Condition that impacts hemodynamic stability (such as autonomic dysfunction, orthostatic intolerance)
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Chronic renal insufficiency
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Chronic or recurrent illness that can affect hydration or volume status. This may include conditions associated with decreased nutritional intake or increased volume loss
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Bone fracture within 6 months prior to screening (within 2 months for fracture of digits)
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Any disease or condition that, in the opinion of the Investigator or Medical Monitor, may make the participant unlikely to fully complete the trial, may confound interpretation of trial results, or may present undue risk from receiving investigational product
- Significant electrocardiogram abnormalities, including evidence of a previous myocardial infarction, left ventricular hypertrophy, flat T waves (particularly in the inferior leads) or more than minor non-specific ST-T wave changes or:
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QRS >90 milliseconds (msec)
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QT interval corrected using Fridericia's formula (QTcF) >440 msec
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PR interval >170 msec
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Complete right or left bundle branch block
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Requires, or anticipated to require, chronic (> 4 weeks) or repeated treatment (more than twice/year) with oral corticosteroids during participation in the trial (low and mid-dose inhaled corticosteroids are allowed with Medical Monitor approval. High-dose inhaled corticosteroids are not allowed)
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Use of medication known to prolong the QT/QTc interval (https://crediblemeds.org/. Note: Only medications on the Known Risk list are excluded, not those on the Possible or Conditional Risk lists). Prior use of such medications is allowed if participant has sufficient wash-out period (minimum 7 days or 5 half-lives, whichever was longer) and a normal QT/QTc interval on ECG.
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Ongoing treatment with any medication that affects blood pressure or heart rate
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Known hypersensitivity to the components of the investigational medicinal product (trehalose, tris(hydroxymethyl)aminomethane, succinate and PEG)
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Any other reason that in the opinion of the Investigator or Medical Monitor would prevent the child from complying with the trial requirements, prevent successful completion of the trial, or prevent successful interpretation of trial data • This could include family situations, comorbid conditions, or medications that might impact safety or be considered confounding
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Ascendis Pharma Investigational Site | Beijing | China | 100045 | |
| 2 | Ascendis Pharma Investigational Site | Guangzhou | China | 510080 | |
| 3 | Ascendis Pharma Investigational Site | Hangzhou | China | 310053 | |
| 4 | Ascendis Pharma Investigational Site | Shanghai | China | 20082 | |
| 5 | Ascendis Pharma Investigational Site | Shenzhen | China | 518053 | |
| 6 | Ascendis Pharma Investigational Site | Wuhan | China | 430030 |
Sponsors and Collaborators
- Ascendis Pharma A/S
Investigators
- Study Director: Marie-Louise Hartoft-Nielsen, MD, PhD, Ascendis Pharma
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- TCC-204