The Effect of Contingent Value Rights on Drug Approval in Biopharma M&A Open Access

Huddleston, Grant (Spring 2026)

Permanent URL: https://etd.library.emory.edu/concern/etds/4j03d127b?locale=en
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Abstract

Opaque assets in mergers and acquisitions (M&A) create the need for unique transaction structures such as contingent value rights (CVRs) and earnouts. Prior research exposes two main functions of these contingent contracts. The first is to align post acquisitions incentives and retain human capital. The second is to bridge valuation disagreements, allowing inherently riskier assets to sell by spreading uncertainty across parties. The capital-intensive and risk-centric biopharmaceutical industry makes it an ideal setting to explore these functions. This paper aims to address the gap in M&A contracting literature by examining CVRs in biopharmaceutical acquisitions to analyze how contingent payment structures influence drug approval.

This paper compiles 313 biopharma transactions from Evaluate Pharma’s transaction database and assesses their post-acquisition success measure through primary asset approval. The data is comprised of 91 transactions structured with a CVR and 222 with upfront payment. It then models out a linear probability model (LPM), logit, and propensity score model (PSM) to compare the percentage of approved deals. The regression models control for three main determinants of drug approval as found in the literature: inherent drug risk, resource risk, and timing risk. These models produce 13% to 19% lower drug approval in CVR transactions, indicating that contingent contracting in biopharma is primarily used to bridge valuation disagreements and thus is more densely used in transactions with greater underlying risk. While this does not refute the possibility of an incentive aligning hypothesis, the findings provide empirical support that CVRs in biopharma transactions serve to bridge valuation and spread risk for assets with extreme uncertainty.

Table of Contents

Introduction

Introduction to Biopharma Industry

Relevant Literature

Adverse Selection and Asymmetric Information in M&A

The Lemons Problem and Medium of Exchange

Earnouts as Extended Contingent Contracting

Contingent Value Rights: Theory and Mechanisms

CVR Structure and Biopharma Context

The Incentive Alignment Hypothesis

The Adverse Selection and Risk Signaling Hypothesis

Competing Hypotheses

Determinants of Drug Approval Success

Overview of Approval Success Rates

Inherent Drug Risk and Therapeutic Characteristics

Size, Experience, and Capital

Time and Evolution of Regulatory Processes

Research Gap and Synthesis

Theoretical Framework

Construction of Dataset for Empirical Analysis

Transaction Data Collection

Drug Approval Data

CVR Variable Construction

Drug Approval Variable Construction

Control Variables Data

Control Variable Selection

Phase at Deal Close Construction

Therapeutic Area Construction

Log of Deal Size Construction

Age of Deal Construction

Summary Statistics and Initial Observations

Variable Distribution Preliminary

Empirical Assessment and Competing Hypotheses

Empirical Design and Methodology

Linear Probability Model

Logit Model

Propensity Score Matching

Results

Linear Probability Regression

Logit Regression

Propensity Score Matching Results

Covariate Balance

ATT Estimates

Illustrative Case Study

Roche’s acquisition of Trophos: High Common Uncertainty and CVR Usage

Roche’s acquisition of Ignyta: Low Common Uncertainty and Fixed-Price Contract

Hypothesis 2: Theoretical Framework in Context

Conclusion

Appendix

Supplemental Heterogeneity Analysis Tables and Figures

Bibliography

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