Approval Probability
TA Base Rate
Adjusted LOA
ML Risk
NNC0487-0111 subcutanous · 1 trial · 1 indication
percent point
| Arm | Type | Description |
|---|---|---|
| Placebo subcutaneous | PLACEBO_COMPARATOR | Placebo for subcutaneous treatment |
| NNC0487-0111 subcutaneous dose 1 | EXPERIMENTAL | NNC0487-0111 subcutaneous dose 1 treatment |
| NNC0487-0111 subcutaneous dose 2 | EXPERIMENTAL | NNC0487-0111 subcutaneous dose 2 treatment |
| NNC0487-0111 subcutaneous dose 3 | EXPERIMENTAL | NNC0487-0111 subcutaneous dose 3 treatment |
| NNC0487-0111 subcutaneous dose 4 | EXPERIMENTAL | NNC0487-0111 subcutaneous dose 4 treatment |
| NNC0487-0111 subcutaneous dose 5 | EXPERIMENTAL | NNC0487-0111 subcutaneous dose 5 treatment |
| NNC0487-0111 subcutaneous dose 6 | EXPERIMENTAL | NNC0487-0111 subcutaneous dose 6 treatment |
| Placebo oral | PLACEBO_COMPARATOR | Placebo for oral treatment |
| NNC0487-0111 oral dose 1 | EXPERIMENTAL | NNC0487-0111 oral dose 1 treatment |
| NNC0487-0111 oral dose 2 | EXPERIMENTAL | NNC0487-0111 oral dose 2 treatment |
| NNC0487-0111 oral dose 3 | EXPERIMENTAL | NNC0487-0111 oral dose 3 treatment |
| Name | Type | Description |
|---|---|---|
| NNC0487-0111 subcutanous | DRUG | NNC0487-0111 administered subcutanously (under the skin) |
| Placebo (NNC0487-0111 subcutanous) | DRUG | NNC0487-0111 placebo administered subcutanously (under the skin) |
| NNC0487-0111 oral | DRUG | NNC0487-0111 administered orally (in the mouth) |
| Placebo (NNC0487-0111 oral) | DRUG | NNC0487-0111 placebo administered orally (in the mouth) |
Inclusion Criteria: * Male or female, aged 18-75 years (both inclusive) at the time of signing the informed consent. * Diagnosed with type 2 diabetes mellitus greater or equal to 180 days before screening. * Stable daily dose(s) greater or equal to 90 days before screening of the following antidiab...
| Company | Ticker | Trials | Lead Phase | Drugs |
|---|---|---|---|---|
| FibroBiologics, Inc. | FBLG | 1 | PHASE1 | Undisclosed |
| MiMedx Group, Inc. | MDXG | 2 | N/A | Undisclosed |
| Integra LifeSciences Holdings Corporation | IART | 1 | N/A | Undisclosed |
| Organogenesis Holdings, Inc. Class A | ORGO | 1 | N/A | Undisclosed |
| Healthcare Services Group, Inc. | HCSG | 1 | N/A | Undisclosed |
NNC0487-0111 subcutaneous is an investigational small molecule being developed for the treatment of Type 2 Diabetes (T2D). It is designed to lower blood sugar levels in people with this condition. The drug is administered subcutaneously and is currently in Phase 2 clinical development, though it remains investigational and not yet approved.
The specific molecular target of NNC0487-0111 is not disclosed in the available information. As a small molecule, it is being studied for its ability to lower blood sugar in patients with Type 2 Diabetes, but the exact biological pathway it acts on has not been publicly detailed.
NNC0487-0111 is being developed by Novo Nordisk A/S, a pharmaceutical company listed on the stock exchange under the ticker symbol NVO. Novo Nordisk is conducting clinical research to evaluate the safety and efficacy of this investigational drug for Type 2 Diabetes.
NNC0487-0111 is currently in Phase 2 clinical development. It is an investigational drug, meaning it has not been approved by regulatory authorities. The Phase 2 trial has been completed, and the drug is being studied for its ability to lower blood sugar in people with Type 2 Diabetes.
NNC0487-0111 has been studied in one completed Phase 2 clinical trial, registered under the identifier NCT06542874. This randomized, double-blind, placebo-controlled study enrolled 448 participants with Type 2 Diabetes and evaluated how well different doses of the medicine lower blood sugar. The trial was conducted across multiple countries, including the United States, Japan, and several European nations.
No alternative names for NNC0487-0111 have been disclosed in the available information. The drug is identified solely by its development code, NNC0487-0111, and is being investigated by Novo Nordisk for the treatment of Type 2 Diabetes.