Enalapril Maleate Drug Asset Due Diligence Report 2026

This Enalapril Maleate Drug Asset Due Diligence Report was built with PatSnap Life Sciences MCP workflows. Drug & Asset MCP establishes identity, ownership and stage; Clinical Trials MCP checks design, endpoints and readouts; Company & Deal Intelligence MCP reconstructs transaction precedent. Explore the MCP servers used in this report.

Decision date: 15 July 2026. Currency fields are presented in US$ millions as returned by the deal dataset. This is a screening memorandum, not legal, medical, patent or investment advice.

Approved

Highest phase

148

Registered trials

Result records

Matched deals

Executive recommendation: GO

Decision memo

Advance diligence: development maturity and available evidence support continued investment, subject to indication-specific safety, IP, and commercial gates.

The central underwriting question is whether Enalapril Maleate can convert its Small molecule drug profile and ACE biology into clinically meaningful differentiation while preserving an investable safety, IP and commercial position.

1. Asset identity and development status

Asset	Enalapril Maleate (query alias: enalapril)
Modality / target	Small molecule drug; ACE; ACE inhibitors
Highest global status	Approved
Originator	Bausch Health Cos., Inc.
Active developers	Merck Sharp & Dohme Corp., Wockhardt Ltd., Proveca Pharma Ltd.

The MCP disease footprint includes Ventricular Dysfunction, Left, Angina Pectoris, Myocardial Infarction. The highest-phase flag is a useful orientation point, but the licensing case depends on indication-level evidence and rights, not the global label alone.

2. Clinical program: design and endpoint audit

Registry	Phase	Status	Enrollment	Lead primary endpoint
NCT07547878	Phase 4	Not yet recruiting	64	On-study retention rate at 6 months
ChiCTR2500112318	Phase 4	Pending	25	Blood Press
NCT07363343	Not Applicable	Recruiting	200	Composite postpartum hypertension treatment failure within 6 weeks postpartum

The trial set should be diligenced for randomization, comparator relevance, endpoint hierarchy, analysis population, multiplicity, geographic mix and readout timing. For early-stage studies, safety and dose selection can be as decision-critical as response rate.

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3. Clinical readouts: what is known

Evidence gap

The Clinical Trials MCP returned no matched public result record. This is a gating diligence gap, not evidence of failure.

These fields are structured evidence signals, not a substitute for statistical review. The next diligence pass should reconcile denominators, confidence intervals, follow-up, censoring, dose cohorts and treatment-emergent toxicity against the original abstract, registry and protocol.

4. Market and competitive position

Enalapril Maleate addresses Ventricular Dysfunction, Left, Angina Pectoris, Myocardial Infarction. Commercial attractiveness rests on addressable biomarker-positive patients, treatment-line placement, duration, administration burden, pricing and displacement of entrenched standards. The modality—Small molecule drug—must demonstrate a benefit large enough to offset class-specific safety and operational costs.

The strongest market-validation signal in this screen is partner behavior: 8 matched transaction record(s) indicate that sophisticated counterparties have assigned strategic value to the asset or its rights. That does not establish net present value; probability of success, remaining R&D spend, royalties, cost sharing and territorial scope still need modeling.

5. Transaction precedent and economics

Transaction-scope note: No direct asset-specific transaction was returned. The table below shows target-level comparable: ACE records as comparable precedents only.

Date	Transaction	Phase at deal	Disclosed economics
2021-07-20	Pharmanovia expands strategic collaboration with M8 Pharmaceuticals in Latin America	Approved	Financial terms not disclosed
	AstraZeneca divests rights to established hypertension medicines	Approved	US$350.0M upfront; US$40.0M milestones; US$390.0M stated total
2019-02-28	Adhera Therapeutics and Alyvant strike deal for Prestalia	Approved	Financial terms not disclosed

Headline values are not directly comparable. Diligence should normalize upfront cash, equity, development and sales milestones, tiered royalties, opt-in mechanics, cost sharing, change-of-control clauses and geography.

6. IP and freedom-to-operate screen

The milestone feed surfaced a patent-application signal described as “Pharmaceutical composition containing bisoprolol and enalapril and process thereof”. The milestone feed surfaced a patent-application signal described as “Preparation method of enalapril maleate and intermediate thereof”. The milestone feed surfaced a patent-application signal described as “Enalapril maleate and furosemide compound tablet, preparation method and application thereof”.

The claim chart should separately test composition or sequence coverage, formulation and dosing, indication and biomarker claims, combinations, manufacturing know-how, prosecution history, term extensions and third-party blocking rights. Confirm that licensed patents, data and know-how track every granted territory and field.

7. Principal risks and diligence gates

Therapeutic index across KRAS/BRAF mutation subgroups
On-target toxicity and adaptive MAPK resistance
Lack of matched efficacy results in the current MCP result set

Cross-functional diligence should also test CMC comparability, supply chain, pharmacovigilance, regulatory correspondence, data integrity, investigator concentration, partner obligations and change-of-control restrictions.

8. Final go/no-go memorandum

GO