Last reviewed 2026-05-31 · How we verify

Drug: Bionetide

Biomed Industries, Inc. · Phase 2 active Small molecule ✓ Verified May 2026 Quality 0/100

Drug: Bionetide is a Small molecule drug developed by Biomed Industries, Inc.. It is currently in Phase 2 development. Also known as: NA-921.

Bionetide is a small molecule drug being studied in a Phase 2/3 clinical trial for the treatment of Rett Syndrome. The trial, NCT06849973, is a randomized, double-blind, placebo-controlled study of Bionetide's efficacy and safety in girls and women with Rett Syndrome.

Likelihood of approval

15.3% vs 15.3% industry baseline

If approved by FDA: likely 2031–2034

Steps remaining: Phase 3 → NDA/BLA submission

Confidence: Medium

Why this estimate

Baseline phase 2 → approval rate +15.3pp
Industry-wide phase 2 drugs reach approval ~15.3% of the time (BIO/Informa 2023 industry benchmark across all therapeutic areas).

Predicted approval windows by jurisdiction (conditional on FDA approval)

Regulator	Country	Likely year	Lag vs FDA
FDA	US	2031–2034	—
EMA	EU	2032–2035	+0.7 yr
MHRA	GB	2032–2035	+0.7 yr
Health Canada	CA	2032–2036	+0.9 yr
TGA	AU	2032–2036	+1.2 yr
PMDA	JP	2032–2036	+1.5 yr
NMPA	CN	2033–2037	+2.3 yr
MFDS	KR	2032–2036	+1.4 yr
CDSCO	IN	2032–2037	+1.8 yr
ANVISA	BR	2033–2037	+2.3 yr

Hover any row for the lag rationale. Lag estimates are reduced when the drug has FDA Breakthrough or EMA PRIME designation (sponsors file globally in parallel).

Estimate based on the BIO/Informa industry phase transition rates plus per-drug modifiers for therapeutic area, sponsor type, FDA designations, mechanism, and trial design. Per-jurisdiction lags from Tufts CSDD international approval studies. Not investment, clinical or regulatory advice. Methodology: /methodology#likelihood.

At a glance

Generic name	Drug: Bionetide
Also known as	NA-921
Sponsor	Biomed Industries, Inc.
Modality	Small molecule
Phase	Phase 2

Approved indications

No approved indications tracked.

Common side effects

No common side effects on file.

Key clinical trials

To Study the Efficacy & Safety of Oral NA-921 (Bionetide) in Girls and Women with Rett Syndrome (PHASE2, PHASE3)

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

Source	Used for
ClinicalTrials.gov	Trial enrolment, design, endpoints, results

Competitive intelligence

For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape:

Drug: Bionetide CI brief — competitive landscape report
Drug: Bionetide updates RSS · CI watch RSS
Biomed Industries, Inc. portfolio CI

Frequently asked questions about Drug: Bionetide

What is Drug: Bionetide?

Drug: Bionetide is a Small molecule drug developed by Biomed Industries, Inc..

Who makes Drug: Bionetide?

Drug: Bionetide is developed by Biomed Industries, Inc. (see full Biomed Industries, Inc. pipeline at /company/biomed-industries-inc).

Is Drug: Bionetide also known as anything else?

Drug: Bionetide is also known as NA-921.

What development phase is Drug: Bionetide in?

Drug: Bionetide is in Phase 2.

Manufacturer: Biomed Industries, Inc. — full pipeline
Also known as: NA-921

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing